A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520276



Internal ID15100883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:24649588..25027423hg38UCSC Ensembl
Innerchr7:24689207..25067042hg19UCSC Ensembl
Innerchr7:24655732..25033567hg18UCSC Ensembl
Innerchr7:24462447..24840282hg17UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38377836
hg19377836
hg18377836
hg17377836
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697320
Samples
Known GenesDFNA5, MPP6, OSBPL3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520276
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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