A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3647019



Internal ID18945300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:110355926..110460888hg38UCSC Ensembl
Innerchr5:109691627..109796589hg19UCSC Ensembl
Innerchr5:109719526..109824488hg18UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg38104963
hg19104963
hg18104963
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1026064
Supporting Variants
Samples
Known GenesTMEM232
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3647019
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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