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dbVar

Database of genomic structural variation

nsv5653729

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: 127 SVs from 30 studies. See in: genome view

Submitted genomic72,347,196-72,347,196

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5653729	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000015.10	Chr15	72,347,196	72,347,196
nsv5653729	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000015.9	Chr15	72,639,537	72,639,537

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17083038	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
nssv17083038	Submitted genomic		NC_000015.10:g.723 47196_72347197ins3 22	GRCh38 (hg38)		NC_000015.10	Chr15	72,347,196	72,347,196
nssv17083038	Remapped	Perfect	NC_000015.9:g.7263 9537_72639538ins32 2	GRCh37.p13	First Pass	NC_000015.9	Chr15	72,639,537	72,639,537

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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