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dbVar

Database of genomic structural variation

nsv6105198

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:34,119

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: 261 SVs from 43 studies. See in: genome view

Submitted genomic121,935,054-121,969,172

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6105198	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	121,935,054	121,969,172
nsv6105198	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	121,270,749	121,304,867

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17541674	inversion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17541674	Submitted genomic		NC_000005.10:g.121 935054_121969172in v	GRCh38 (hg38)		NC_000005.10	Chr5	121,935,054	121,969,172
nssv17541674	Remapped	Perfect	NC_000005.9:g.1212 70749_121304867inv	GRCh37.p13	First Pass	NC_000005.9	Chr5	121,270,749	121,304,867

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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