Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv5643536

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: 394 SVs from 48 studies. See in: genome view

Submitted genomic10,639,588-10,639,588

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5643536	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	10,639,588	10,639,588
nsv5643536	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	10,639,700	10,639,700

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17136352	insertion	SAMN00001695	Sequencing	Sequence alignment	6,153

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17136352	Submitted genomic		NC_000005.10:g.106 39588_10639589ins3 73	GRCh38 (hg38)		NC_000005.10	Chr5	10,639,588	10,639,588
nssv17136352	Remapped	Perfect	NC_000005.9:g.1063 9700_10639701ins37 3	GRCh37.p13	First Pass	NC_000005.9	Chr5	10,639,700	10,639,700

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.

You are here: NCBI