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dbVar

Database of genomic structural variation

nsv6108619

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:90,335

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: 348 SVs from 52 studies. See in: genome view

Submitted genomic63,693,672-63,784,006

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6108619	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000016.10	Chr16	63,693,672	63,784,006
nsv6108619	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000016.9	Chr16	63,727,576	63,817,910

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17630860	inversion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17630860	Submitted genomic		NC_000016.10:g.636 93672_63784006inv	GRCh38 (hg38)		NC_000016.10	Chr16	63,693,672	63,784,006
nssv17630860	Remapped	Perfect	NC_000016.9:g.6372 7576_63817910inv	GRCh37.p13	First Pass	NC_000016.9	Chr16	63,727,576	63,817,910

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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