Warning: The NCBI web site requires JavaScript to function. more...

dbVar

Database of genomic structural variation

nsv6131993

Organism: Homo sapiens

Study:nstd213 (Pham et al. 2021)
Variant Type:inversion
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:45,809

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: 393 SVs from 75 studies. See in: genome view

Remapped(Score: Perfect):1,894,039-1,939,847

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nsv6131993	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000011.10	Chr11	1,894,039	1,894,040	1,939,826	1,939,847
nsv6131993	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000011.9	Chr11	1,915,269	1,915,270	1,961,056	1,961,077

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17679098	inversion	SAMN20524663	Sequencing	Paired-end mapping	244

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nssv17679098	Remapped	Perfect	NC_000011.10:g.(18 94039_1894040)_(19 39826_1939847)inv	GRCh38.p12	First Pass	NC_000011.10	Chr11	1,894,039	1,894,040	1,939,826	1,939,847
nssv17679098	Submitted genomic		NC_000011.9:g.(191 5269_1915270)_(196 1056_1961077)inv	GRCh37 (hg19)		NC_000011.9	Chr11	1,915,269	1,915,270	1,961,056	1,961,077

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

You are here: NCBI