A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891688



Internal ID19186084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:81950922..81974953hg38UCSC Ensembl
Outerchr9:81950922..81974953hg38UCSC Ensembl
Innerchr9:84565837..84589868hg19UCSC Ensembl
Outerchr9:84565837..84589868hg19UCSC Ensembl
Innerchr9:83755657..83779688hg18UCSC Ensembl
Outerchr9:83755657..83779688hg18UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3824032
hg1924032
hg1824032
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797875
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891688
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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