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dbVar

Database of genomic structural variation

nsv7099292

Organism: Homo sapiens

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

Variant Calls:2
Validation:Not tested
Clinical Assertions: No
Region Size:29,630

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: 213 SVs from 32 studies. See in: genome view

Remapped(Score: Perfect):93,838,068-93,867,697

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nsv7099292	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000013.11	Chr13	93,838,068	93,867,697
nsv7099292	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000013.10	Chr13	94,490,321	94,519,950

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18793006	duplication	SNP array	SNP genotyping analysis
nssv18793039	duplication	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
nssv18793006	Remapped	Perfect	NC_000013.11:g.(93 838068_?)_(?_93867 697)dup	GRCh38.p12	First Pass	NC_000013.11	Chr13	93,838,068	93,867,697
nssv18793039	Remapped	Perfect	NC_000013.11:g.(93 838068_?)_(?_93867 697)dup	GRCh38.p12	First Pass	NC_000013.11	Chr13	93,838,068	93,867,697
nssv18793006	Submitted genomic		NC_000013.10:g.(94 490321_?)_(?_94519 950)dup	GRCh37 (hg19)		NC_000013.10	Chr13	94,490,321	94,519,950
nssv18793039	Submitted genomic		NC_000013.10:g.(94 490321_?)_(?_94519 950)dup	GRCh37 (hg19)		NC_000013.10	Chr13	94,490,321	94,519,950

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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