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

dbVar

Database of genomic structural variation

nsv6283334

Organism: Homo sapiens

Study:nstd214 (Naslavsky et al. 2022)
Variant Type:insertion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:1

Publication(s):Naslavsky et al. 2022

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: 117 SVs from 28 studies. See in: genome view

Submitted genomic87,857,803-87,857,803

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6283334	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000009.12	Chr9	87,857,803	87,857,803
nsv6283334	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000009.11	Chr9	90,472,718	90,472,718

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17906180	insertion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17906180	Submitted genomic		NC_000009.12:g.878 57803_87857804ins8 0	GRCh38 (hg38)		NC_000009.12	Chr9	87,857,803	87,857,803
nssv17906180	Remapped	Perfect	NC_000009.11:g.904 72718_90472719ins8 0	GRCh37.p13	First Pass	NC_000009.11	Chr9	90,472,718	90,472,718

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call ID	Allele Frequency (AF)	Allele Count (AC)	Allele Number (AN)
nssv17906180	0.003	8	2336

You are here: NCBI