A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4756n100



Internal ID20156372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:62681587..62712793hg38UCSC Ensembl
chr3:62667262..62698468hg19UCSC Ensembl
chr3:62642302..62673508hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg3831207
hg1931207
hg1831207
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv999644, nsv1013624, nsv1013155, nsv1009465, nsv1006740
Samples
Known GenesCADPS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4756n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss28
Observed Complex0
Frequencyn/a


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