A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1626n100



Internal ID22787713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:32664185..32783365hg38UCSC Ensembl
chr13:33238322..33357503hg19UCSC Ensembl
chr13:32136322..32255503hg18UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg38119181
hg19119182
hg18119182
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1050703, nsv1037381
Samples
Known GenesPDS5B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1626n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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