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dbVar

Database of genomic structural variation

nsv6133372

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:113,246

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: 641 SVs from 59 studies. See in: genome view

Remapped(Score: Perfect):29,539,045-29,652,290

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
nsv6133372	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000018.10	Chr18	29,539,045	29,539,071	29,652,264	29,652,290
nsv6133372	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000018.9	Chr18	27,119,010	27,119,036	27,232,229	27,232,255

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17682654	inversion	SAMN20524657	Sequencing	Paired-end mapping	656

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nssv17682654	Remapped	Perfect	NC_000018.10:g.(29 539045_29539071)_( 29652264_29652290) inv	GRCh38.p12	First Pass	NC_000018.10	Chr18	29,539,045	29,539,071	29,652,264	29,652,290
nssv17682654	Submitted genomic		NC_000018.9:g.(271 19010_27119036)_(2 7232229_27232255)i nv	GRCh37 (hg19)		NC_000018.9	Chr18	27,119,010	27,119,036	27,232,229	27,232,255

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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