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dbVar

Database of genomic structural variation

nsv4757377

Organism: Homo sapiens

Study:nstd199 (Quan et al. 2021)
Variant Type:inversion
Method Type:Sequencing
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:90,852

Publication(s):Quan et al. 2021

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

Remapped(Score: Perfect):72,996,084-73,086,935

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4757377	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000023.11	ChrX	72,996,084	73,086,935
nsv4757377	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000023.10	ChrX	72,215,923	72,306,774

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16260747	inversion	Sequencing	Split read mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16260747	Remapped	Perfect	NC_000023.11:g.729 96084_73086935inv	GRCh38.p12	First Pass	NC_000023.11	ChrX	72,996,084	73,086,935
nssv16260747	Submitted genomic		NC_000023.10:g.722 15923_72306774inv	GRCh37 (hg19)		NC_000023.10	ChrX	72,215,923	72,306,774

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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