A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1702n100



Internal ID22787789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:68053967..68237516hg38UCSC Ensembl
chr13:68628099..68811648hg19UCSC Ensembl
chr13:67526100..67709649hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg38183550
hg19183550
hg18183550
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1052880, nsv1054527
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)dgv1702n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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