A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv76e55



Internal ID22761026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:62707806..63063144hg38UCSC Ensembl
chr13:63281939..63637277hg19UCSC Ensembl
chr13:62179940..62535278hg18UCSC Ensembl
chr13:62179940..62535278hg17UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38355339
hg19355339
hg18355339
hg17355339
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv34296, esv34669
SamplesNA18973, NA18956
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)dgv76e55
Frequency
Sample Size771
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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