A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788211



Internal ID18823114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:892241..1158171hg38UCSC Ensembl
Innerchr9:892241..1158171hg19UCSC Ensembl
Innerchr9:882241..1148171hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38265931
hg19265931
hg18265931
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891516
Supporting Variants
Samples
Known GenesDMRT1, DMRT2, DMRT3
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=94
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788211
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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