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dbVar

Database of genomic structural variation

nsv7099299

Organism: Homo sapiens

Study:nstd231 (Ali et al. 2023)
Variant Type:copy number variation
Method Type:SNP array
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:5,299

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: 428 SVs from 25 studies. See in: genome view

Remapped(Score: Perfect):31,440,509-31,445,807

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nsv7099299	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000023.11	ChrX	31,440,509	31,445,807
nsv7099299	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000023.10	ChrX	31,458,626	31,463,924

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18792917	deletion	SNP array	SNP genotyping analysis

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nssv18792917	Remapped	Perfect	NC_000023.11:g.(31 440509_?)_(?_31445 807)del	GRCh38.p12	First Pass	NC_000023.11	ChrX	31,440,509	31,445,807
nssv18792917	Submitted genomic		NC_000023.10:g.(31 458626_?)_(?_31463 924)del	GRCh37 (hg19)		NC_000023.10	ChrX	31,458,626	31,463,924

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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