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

dbVar

Database of genomic structural variation

nsv5636388

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: 206 SVs from 27 studies. See in: genome view

Submitted genomic125,731,795-125,731,795

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5636388	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	125,731,795	125,731,795
nsv5636388	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	127,420,364	127,420,364

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17067649	insertion	HG03486	Sequencing	Sequence alignment	4,355

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17067649	Submitted genomic		NC_000010.11:g.125 731795_125731796in s2337	GRCh38 (hg38)		NC_000010.11	Chr10	125,731,795	125,731,795
nssv17067649	Remapped	Perfect	NC_000010.10:g.127 420364_127420365in s2337	GRCh37.p13	First Pass	NC_000010.10	Chr10	127,420,364	127,420,364

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