A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891683



Internal ID19186079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:73182919..73195477hg38UCSC Ensembl
Outerchr9:73182919..73195477hg38UCSC Ensembl
Innerchr9:75797835..75810393hg19UCSC Ensembl
Outerchr9:75797835..75810393hg19UCSC Ensembl
Innerchr9:74987655..75000213hg18UCSC Ensembl
Outerchr9:74987655..75000213hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3812559
hg1912559
hg1812559
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782416
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891683
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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