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dbVar

Database of genomic structural variation

nsv5661513

Organism: Homo sapiens

Study:nstd207 (Ebert et al. 2021)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Ebert et al. 2021

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: 453 SVs from 46 studies. See in: genome view

Submitted genomic1,185,658-1,185,658

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5661513	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	1,185,658	1,185,658
nsv5661513	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	1,235,658	1,235,658

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17082617	insertion	SAMN00006579	Sequencing	Sequence alignment	23,265

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17082617	Submitted genomic		NC_000016.10:g.118 5658_1185659ins170 7	GRCh38 (hg38)		NC_000016.10	Chr16	1,185,658	1,185,658
nssv17082617	Remapped	Perfect	NC_000016.9:g.1235 658_1235659ins1707	GRCh37.p13	First Pass	NC_000016.9	Chr16	1,235,658	1,235,658

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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