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dbVar

Database of genomic structural variation

nsv6132401

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:31,123

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: 189 SVs from 41 studies. See in: genome view

Remapped(Score: Perfect):79,674,042-79,705,164

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
nsv6132401	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000012.12	Chr12	79,674,042	79,674,045	79,705,163	79,705,164
nsv6132401	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000012.11	Chr12	80,067,822	80,067,825	80,098,943	80,098,944

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17683265	inversion	SAMN20524655	Sequencing	Paired-end mapping	909

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nssv17683265	Remapped	Perfect	NC_000012.12:g.(79 674042_79674045)_( 79705163_79705164) inv	GRCh38.p12	First Pass	NC_000012.12	Chr12	79,674,042	79,674,045	79,705,163	79,705,164
nssv17683265	Submitted genomic		NC_000012.11:g.(80 067822_80067825)_( 80098943_80098944) inv	GRCh37 (hg19)		NC_000012.11	Chr12	80,067,822	80,067,825	80,098,943	80,098,944

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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