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

dbVar

Database of genomic structural variation

nsv5636663

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: 195 SVs from 43 studies. See in: genome view

Submitted genomic176,305,314-176,305,314

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5636663	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	176,305,314	176,305,314
nsv5636663	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	175,732,317	175,732,317

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17122114	insertion	HG02492	Sequencing	Sequence alignment	982

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17122114	Submitted genomic		NC_000005.10:g.176 305314_176305315in s1407	GRCh38 (hg38)		NC_000005.10	Chr5	176,305,314	176,305,314
nssv17122114	Remapped	Perfect	NC_000005.9:g.1757 32317_175732318ins 1407	GRCh37.p13	First Pass	NC_000005.9	Chr5	175,732,317	175,732,317

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