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

dbVar

Database of genomic structural variation

nsv7059394

Organism: Homo sapiens

Study:nstd229 (Jun et al. 2023)
Variant Type:inversion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:654,141

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: 1998 SVs from 98 studies. See in: genome view

Submitted genomic16,560,428-17,214,568

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv7059394	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000017.11	Chr17	16,560,428	17,214,568
nsv7059394	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000017.10	Chr17	16,463,742	17,117,882

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18756177	inversion	Sequencing	Split read and paired-end mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv18756177	Submitted genomic		NC_000017.11:g.165 60428_17214568inv	GRCh38 (hg38)		NC_000017.11	Chr17	16,560,428	17,214,568
nssv18756177	Remapped	Perfect	NC_000017.10:g.164 63742_17117882inv	GRCh37.p13	First Pass	NC_000017.10	Chr17	16,463,742	17,117,882

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)
nssv18756177	0.001	350	272828

You are here: NCBI