A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3264n100



Internal ID22789351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:52876233..53237046hg38UCSC Ensembl
chr17:50953593..51314407hg19UCSC Ensembl
chr17:48308592..48669406hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38360814
hg19360815
hg18360815
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1062893, nsv1060325, nsv1059575
Samples
Known GenesC17orf112
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3264n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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