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dbVar

Database of genomic structural variation

nsv6136289

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:153,566

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: 550 SVs from 58 studies. See in: genome view

Remapped(Score: Perfect):138,235,214-138,388,779

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
nsv6136289	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	138,235,214	138,235,216	138,388,777	138,388,779
nsv6136289	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000008.10	Chr8	139,247,457	139,247,459	139,401,020	139,401,022

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17682436	inversion	SAMN20524662	Sequencing	Paired-end mapping	1,603

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nssv17682436	Remapped	Perfect	NC_000008.11:g.(13 8235214_138235216) _(138388777_138388 779)inv	GRCh38.p12	First Pass	NC_000008.11	Chr8	138,235,214	138,235,216	138,388,777	138,388,779
nssv17682436	Submitted genomic		NC_000008.10:g.(13 9247457_139247459) _(139401020_139401 022)inv	GRCh37 (hg19)		NC_000008.10	Chr8	139,247,457	139,247,459	139,401,020	139,401,022

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

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