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dbVar

Database of genomic structural variation

nsv3564775

Organism: Homo sapiens

Study:nstd152 (Chaisson et al. 2019)
Variant Type:mobile element insertion
Method Type:Sequencing
Submitted on:GRCh38 (hg38)

Variant Calls:3
Validation:Not tested
Clinical Assertions: No
Region Size:1

Description:Insertion of a SVA mobile element relative to the reference
Publication(s):Chaisson 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: 276 SVs from 34 studies. See in: genome view

Submitted genomic151,626,787-151,626,817

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv3564775	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000007.14	Chr7	151,626,802 (-15, +15)	151,626,802 (-15, +15)
nsv3564775	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000007.13	Chr7	151,323,888 (-15, +15)	151,323,888 (-15, +15)

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Zygosity	Other Calls in this Sample and Study
nssv14338676	sva insertion	SAMN00001694	Sequencing	Sequence alignment	Heterozygous	16,419
nssv14338677	sva insertion	SAMN00001695	Sequencing	Sequence alignment	Heterozygous	15,732
nssv14338678	sva insertion	SAMN00001696	Sequencing	Sequence alignment	Heterozygous	45,591

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv14338676	Submitted genomic		NC_000007.14:g.(15 1626787_151626817) _(151626787_151626 817)ins1240	GRCh38 (hg38)		NC_000007.14	Chr7	151,626,802 (-15, +15)	151,626,802 (-15, +15)
nssv14338677	Submitted genomic		NC_000007.14:g.(15 1626787_151626817) _(151626787_151626 817)ins1240	GRCh38 (hg38)		NC_000007.14	Chr7	151,626,802 (-15, +15)	151,626,802 (-15, +15)
nssv14338678	Submitted genomic		NC_000007.14:g.(15 1626787_151626817) _(151626787_151626 817)ins1240	GRCh38 (hg38)		NC_000007.14	Chr7	151,626,802 (-15, +15)	151,626,802 (-15, +15)
nssv14338676	Remapped	Perfect	NC_000007.13:g.(15 1323873_151323903) _(151323873_151323 903)ins1240	GRCh37.p13	First Pass	NC_000007.13	Chr7	151,323,888 (-15, +15)	151,323,888 (-15, +15)
nssv14338677	Remapped	Perfect	NC_000007.13:g.(15 1323873_151323903) _(151323873_151323 903)ins1240	GRCh37.p13	First Pass	NC_000007.13	Chr7	151,323,888 (-15, +15)	151,323,888 (-15, +15)
nssv14338678	Remapped	Perfect	NC_000007.13:g.(15 1323873_151323903) _(151323873_151323 903)ins1240	GRCh37.p13	First Pass	NC_000007.13	Chr7	151,323,888 (-15, +15)	151,323,888 (-15, +15)

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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