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

dbVar

Database of genomic structural variation

nsv5627581

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: 278 SVs from 54 studies. See in: genome view

Submitted genomic35,797,677-35,797,677

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5627581	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000006.12	Chr6	35,797,677	35,797,677
nsv5627581	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000006.11	Chr6	35,765,454	35,765,454

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17149235	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
nssv17149235	Submitted genomic		NC_000006.12:g.357 97677_35797678ins1 2227	GRCh38 (hg38)		NC_000006.12	Chr6	35,797,677	35,797,677
nssv17149235	Remapped	Perfect	NC_000006.11:g.357 65454_35765455ins1 2227	GRCh37.p13	First Pass	NC_000006.11	Chr6	35,765,454	35,765,454

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