A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4761n100



Internal ID22790848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:65200174..65224765hg38UCSC Ensembl
chr3:65185849..65210440hg19UCSC Ensembl
chr3:65160889..65185480hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3824592
hg1924592
hg1824592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1010665, nsv1003976, nsv1002833, nsv1008150, nsv1002240, nsv1006720, nsv1013922, nsv1013607, nsv1012715, nsv999244, nsv1005360, nsv1002938, nsv1014864, nsv1003199, nsv1001564, nsv1011173, nsv1011108, nsv1013760
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)dgv4761n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss641
Observed Complex0
Frequencyn/a


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