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dbVar

Database of genomic structural variation

nsv6102301

Organism: Homo sapiens

Study:nstd212 (Wu et al. 2021)
Variant Type:inversion
Method Type:Sequencing
Submitted on:GRCh38

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:38,132

Publication(s):Wu 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: 370 SVs from 59 studies. See in: genome view

Submitted genomic35,783,773-35,821,904

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6102301	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	35,783,773	35,821,904
nsv6102301	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	35,018,144	35,056,275

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17635568	inversion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17635568	Submitted genomic		NC_000016.10:g.357 83773_35821904inv	GRCh38 (hg38)		NC_000016.10	Chr16	35,783,773	35,821,904
nssv17635568	Remapped	Perfect	NC_000016.9:g.3501 8144_35056275inv	GRCh37.p13	First Pass	NC_000016.9	Chr16	35,018,144	35,056,275

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.

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