A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1697n100



Internal ID22787784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:63845046..64388006hg38UCSC Ensembl
chr13:64419179..64962138hg19UCSC Ensembl
chr13:63317180..63860139hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38542961
hg19542960
hg18542960
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044946, nsv1037078, nsv1038291, nsv1047229
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)dgv1697n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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