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dbVar

Database of genomic structural variation

nsv6107484

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:72,236

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: 287 SVs from 50 studies. See in: genome view

Submitted genomic121,950,989-122,023,224

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6107484	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000005.10	Chr5	121,950,989	122,023,224
nsv6107484	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000005.9	Chr5	121,286,684	121,358,919

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17544244	inversion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17544244	Submitted genomic		NC_000005.10:g.121 950989_122023224in v	GRCh38 (hg38)		NC_000005.10	Chr5	121,950,989	122,023,224
nssv17544244	Remapped	Perfect	NC_000005.9:g.1212 86684_121358919inv	GRCh37.p13	First Pass	NC_000005.9	Chr5	121,286,684	121,358,919

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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