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

dbVar

Database of genomic structural variation

nsv7076222

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:399,897

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: 1631 SVs from 93 studies. See in: genome view

Submitted genomic28,418,032-28,817,928

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv7076222	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	28,418,032	28,817,928
nsv7076222	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	28,429,353	28,829,249

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18757347	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
nssv18757347	Submitted genomic		NC_000016.10:g.284 18032_28817928inv	GRCh38 (hg38)		NC_000016.10	Chr16	28,418,032	28,817,928
nssv18757347	Remapped	Perfect	NC_000016.9:g.2842 9353_28829249inv	GRCh37.p13	First Pass	NC_000016.9	Chr16	28,429,353	28,829,249

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)
nssv18757347	2.2e-05	6	272934

You are here: NCBI