A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4967n100



Internal ID22791054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:162908772..163442190hg38UCSC Ensembl
chr3:162626560..163159978hg19UCSC Ensembl
chr3:164109254..164642672hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38533419
hg19533419
hg18533419
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1012835, nsv1006015
Samples
Known GenesCT64
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4967n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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