A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655057



Internal ID18606652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:5169879..5215768hg38UCSC Ensembl
Innerchr7:5209510..5255399hg19UCSC Ensembl
Innerchr7:5176036..5221925hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3845890
hg1945890
hg1845890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015639
Supporting Variants
Samples
Known GenesWIPI2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3655057
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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