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dbVar

Database of genomic structural variation

nsv4764886

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:78,280

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

Remapped(Score: Perfect):73,002,372-73,080,651

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4764886	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000023.11	ChrX	73,002,372	73,080,651
nsv4764886	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000023.10	ChrX	72,222,211	72,300,490

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16265884	inversion	Sequencing	Split read mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16265884	Remapped	Perfect	NC_000023.11:g.730 02372_73080651inv	GRCh38.p12	First Pass	NC_000023.11	ChrX	73,002,372	73,080,651
nssv16265884	Submitted genomic		NC_000023.10:g.722 22211_72300490inv	GRCh37 (hg19)		NC_000023.10	ChrX	72,222,211	72,300,490

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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