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dbVar

Database of genomic structural variation

nsv7099196

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:1,257,559

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: 3069 SVs from 86 studies. See in: genome view

Remapped(Score: Perfect):42,172,633-43,430,191

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nsv7099196	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000001.11	Chr1	42,172,633	43,430,191
nsv7099196	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000001.10	Chr1	42,638,304	43,895,862

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18792926	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
nssv18792926	Remapped	Perfect	NC_000001.11:g.(42 172633_?)_(?_43430 191)dup	GRCh38.p12	First Pass	NC_000001.11	Chr1	42,172,633	43,430,191
nssv18792926	Submitted genomic		NC_000001.10:g.(42 638304_?)_(?_43895 862)dup	GRCh37 (hg19)		NC_000001.10	Chr1	42,638,304	43,895,862

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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