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dbVar

Database of genomic structural variation

nsv6133486

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:368,735

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: 1239 SVs from 82 studies. See in: genome view

Remapped(Score: Perfect):190,683,055-191,051,789

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
nsv6133486	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000001.11	Chr1	190,683,055	190,683,071	191,051,773	191,051,789
nsv6133486	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000001.10	Chr1	190,652,185	190,652,201	191,020,903	191,020,919

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis	Other Calls in this Sample and Study
nssv17678319	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
nssv17678319	Remapped	Perfect	NC_000001.11:g.(19 0683055_190683071) _(191051773_191051 789)inv	GRCh38.p12	First Pass	NC_000001.11	Chr1	190,683,055	190,683,071	191,051,773	191,051,789
nssv17678319	Submitted genomic		NC_000001.10:g.(19 0652185_190652201) _(191020903_191020 919)inv	GRCh37 (hg19)		NC_000001.10	Chr1	190,652,185	190,652,201	191,020,903	191,020,919

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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