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dbVar

Database of genomic structural variation

nsv4761608

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:14,708

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: 473 SVs from 35 studies. See in: genome view

Remapped(Score: Good):150,402,694-150,417,401

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv4761608	Remapped	Good	GRCh38.p12	Primary Assembly	First Pass	NC_000023.11	ChrX	150,402,694	150,417,401
nsv4761608	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000023.10	ChrX	149,570,963	149,585,675

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv16268971	inversion	Sequencing	Split read mapping

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv16268971	Remapped	Good	NC_000023.11:g.150 402694_150417401in v	GRCh38.p12	First Pass	NC_000023.11	ChrX	150,402,694	150,417,401
nssv16268971	Submitted genomic		NC_000023.10:g.149 570963_149585675in v	GRCh37 (hg19)		NC_000023.10	ChrX	149,570,963	149,585,675

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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