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dbVar

Database of genomic structural variation

nsv6104561

Organism: Homo sapiens

Study:nstd212 (Wu et al. 2021)
Variant Type:copy number variation
Method Type:Sequencing
Submitted on:GRCh38

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

Publication(s):Wu 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: 382 SVs from 28 studies. See in: genome view

Submitted genomic74,441,032-74,441,121

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv6104561	Submitted genomic		GRCh38 (hg38)	Primary Assembly		NC_000023.11	ChrX	74,441,032	74,441,121
nsv6104561	Remapped	Perfect	GRCh37.p13	Primary Assembly	First Pass	NC_000023.10	ChrX	73,660,867	73,660,956

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17649848	deletion	Sequencing	Sequence alignment

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv17649848	Submitted genomic		NC_000023.11:g.744 41032_74441121del	GRCh38 (hg38)		NC_000023.11	ChrX	74,441,032	74,441,121
nssv17649848	Remapped	Perfect	NC_000023.10:g.736 60867_73660956del	GRCh37.p13	First Pass	NC_000023.10	ChrX	73,660,867	73,660,956

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype and/or allele frequency data can be found on dbVar's FTP site.

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