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dbVar

Database of genomic structural variation

nsv7062698

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:571,806

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: 2487 SVs from 90 studies. See in: genome view

Submitted genomic84,376,803-84,948,608

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv7062698	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	84,376,803	84,948,608
nsv7062698	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	84,410,409	84,982,214

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18756649	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
nssv18756649	Submitted genomic		NC_000016.10:g.843 76803_84948608inv	GRCh38 (hg38)		NC_000016.10	Chr16	84,376,803	84,948,608
nssv18756649	Remapped	Perfect	NC_000016.9:g.8441 0409_84982214inv	GRCh37.p13	First Pass	NC_000016.9	Chr16	84,410,409	84,982,214

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)
nssv18756649	3.2e-05	9	274592

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