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dbVar

Database of genomic structural variation

nsv7099295

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:106,252

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: 789 SVs from 71 studies. See in: genome view

Remapped(Score: Perfect):89,332,862-89,439,113

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Outer Stop
nsv7099295	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000016.10	Chr16	89,332,862	89,439,113
nsv7099295	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000016.9	Chr16	89,399,270	89,505,521

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv18793032	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
nssv18793032	Remapped	Perfect	NC_000016.10:g.(89 332862_?)_(?_89439 113)del	GRCh38.p12	First Pass	NC_000016.10	Chr16	89,332,862	89,439,113
nssv18793032	Submitted genomic		NC_000016.9:g.(893 99270_?)_(?_895055 21)del	GRCh37 (hg19)		NC_000016.9	Chr16	89,399,270	89,505,521

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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