A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2732n100



Internal ID22788819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12554201..12576731hg38UCSC Ensembl
chr16:12648058..12670588hg19UCSC Ensembl
chr16:12555559..12578089hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3822531
hg1922531
hg1822531
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1050925, nsv1044772
Samples
Known GenesSNX29
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv2732n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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