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

dbVar

Database of genomic structural variation

nsv5659660

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: 1186 SVs from 79 studies. See in: genome view

Submitted genomic133,460,509-133,460,509

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv5659660	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000010.11	Chr10	133,460,509	133,460,509
nsv5659660	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000010.10	Chr10	135,274,013	135,274,013

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17068015	insertion	HG03732	Sequencing	Sequence alignment	1,582

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17068015	Submitted genomic		NC_000010.11:g.133 460509_133460510in s57	GRCh38 (hg38)		NC_000010.11	Chr10	133,460,509	133,460,509
nssv17068015	Remapped	Perfect	NC_000010.10:g.135 274013_135274014in s57	GRCh37.p13	First Pass	NC_000010.10	Chr10	135,274,013	135,274,013

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