A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891695



Internal ID19186091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:97162322..97195269hg38UCSC Ensembl
Outerchr9:97162322..97195269hg38UCSC Ensembl
Innerchr9:99924604..99957551hg19UCSC Ensembl
Outerchr9:99924604..99957551hg19UCSC Ensembl
Innerchr9:98964425..98997372hg18UCSC Ensembl
Outerchr9:98964425..98997372hg18UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg3832948
hg1932948
hg1832948
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25785951
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891695
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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