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dbVar

Database of genomic structural variation

nsv3418791

Organism: Homo sapiens

Study:nstd162 (Audano et al. 2019)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38 (hg38)

Variant Calls:8
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Audano et al. 2019

Links to Other Resources

Overlapping Genes

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 279 SVs from 39 studies. See in: genome view

Submitted genomic157,725,990-157,725,990

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv3418791	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	157,725,990	157,725,990
nsv3418791	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	157,518,682	157,518,682

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv14752198	insertion	SAMN09643900	Sequencing	de novo and local sequence assembly	26,631
nssv14759701	insertion	SAMN04229552	Sequencing	de novo and local sequence assembly	24,632
nssv14760283	insertion	SAMN06885952	Sequencing	de novo and local sequence assembly	28,070
nssv14760485	insertion	SAMN05181962	Sequencing	de novo and local sequence assembly	23,563
nssv14762366	insertion	SAMN04251426	Sequencing	de novo and local sequence assembly	22,074
nssv14763336	insertion	SAMN09651199	Sequencing	de novo and local sequence assembly	27,381
nssv14765595	insertion	SAMN05603847	Sequencing	de novo and local sequence assembly	26,021
nssv14766756	insertion	SAMN09690649	Sequencing	de novo and local sequence assembly	21,495

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv14752198	Submitted genomic		NC_000007.14:g.157 725990_157725991in s614	GRCh38 (hg38)		NC_000007.14	Chr7	157,725,990	157,725,990
nssv14759701	Submitted genomic		NC_000007.14:g.157 725990_157725991in s614	GRCh38 (hg38)		NC_000007.14	Chr7	157,725,990	157,725,990
nssv14760283	Submitted genomic		NC_000007.14:g.157 725990_157725991in s614	GRCh38 (hg38)		NC_000007.14	Chr7	157,725,990	157,725,990
nssv14760485	Submitted genomic		NC_000007.14:g.157 725990_157725991in s614	GRCh38 (hg38)		NC_000007.14	Chr7	157,725,990	157,725,990
nssv14762366	Submitted genomic		NC_000007.14:g.157 725990_157725991in s614	GRCh38 (hg38)		NC_000007.14	Chr7	157,725,990	157,725,990
nssv14763336	Submitted genomic		NC_000007.14:g.157 725990_157725991in s614	GRCh38 (hg38)		NC_000007.14	Chr7	157,725,990	157,725,990
nssv14765595	Submitted genomic		NC_000007.14:g.157 725990_157725991in s614	GRCh38 (hg38)		NC_000007.14	Chr7	157,725,990	157,725,990
nssv14766756	Submitted genomic		NC_000007.14:g.157 725990_157725991in s614	GRCh38 (hg38)		NC_000007.14	Chr7	157,725,990	157,725,990
nssv14752198	Remapped	Perfect	NC_000007.13:g.157 518682_157518683in s614NC_000007.13:g .157518682_1575186 83ins614	GRCh37.p13	First Pass	NC_000007.13	Chr7	157,518,682	157,518,682
nssv14759701	Remapped	Perfect	NC_000007.13:g.157 518682_157518683in s614NC_000007.13:g .157518682_1575186 83ins614	GRCh37.p13	First Pass	NC_000007.13	Chr7	157,518,682	157,518,682
nssv14760283	Remapped	Perfect	NC_000007.13:g.157 518682_157518683in s614NC_000007.13:g .157518682_1575186 83ins614	GRCh37.p13	First Pass	NC_000007.13	Chr7	157,518,682	157,518,682
nssv14760485	Remapped	Perfect	NC_000007.13:g.157 518682_157518683in s614NC_000007.13:g .157518682_1575186 83ins614	GRCh37.p13	First Pass	NC_000007.13	Chr7	157,518,682	157,518,682
nssv14762366	Remapped	Perfect	NC_000007.13:g.157 518682_157518683in s614NC_000007.13:g .157518682_1575186 83ins614	GRCh37.p13	First Pass	NC_000007.13	Chr7	157,518,682	157,518,682
nssv14763336	Remapped	Perfect	NC_000007.13:g.157 518682_157518683in s614NC_000007.13:g .157518682_1575186 83ins614	GRCh37.p13	First Pass	NC_000007.13	Chr7	157,518,682	157,518,682
nssv14765595	Remapped	Perfect	NC_000007.13:g.157 518682_157518683in s614NC_000007.13:g .157518682_1575186 83ins614	GRCh37.p13	First Pass	NC_000007.13	Chr7	157,518,682	157,518,682
nssv14766756	Remapped	Perfect	NC_000007.13:g.157 518682_157518683in s614NC_000007.13:g .157518682_1575186 83ins614	GRCh37.p13	First Pass	NC_000007.13	Chr7	157,518,682	157,518,682

Showing 16 of 24

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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