A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891516



Internal ID18839226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:892241..1158171hg38UCSC Ensembl
Outerchr9:892241..1158171hg38UCSC Ensembl
Innerchr9:892241..1158171hg19UCSC Ensembl
Outerchr9:892241..1158171hg19UCSC Ensembl
Innerchr9:882241..1148171hg18UCSC Ensembl
Outerchr9:882241..1148171hg18UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38265931
hg19265931
hg18265931
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788211
Samples
Known GenesDMRT1, DMRT2, DMRT3
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891516
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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