A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3756n100



Internal ID22789843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:34001289..34121610hg38UCSC Ensembl
chr2:34226356..34346677hg19UCSC Ensembl
chr2:34079860..34200181hg18UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38120322
hg19120322
hg18120322
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1001147, nsv1012084, nsv1011569, nsv1009776, nsv1012223
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)dgv3756n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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