A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4772n100



Internal ID22790859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:68670067..68699623hg38UCSC Ensembl
chr3:68719218..68748774hg19UCSC Ensembl
chr3:68801908..68831464hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3829557
hg1929557
hg1829557
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv998169, nsv1007418, nsv1004066
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4772n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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