A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891647



Internal ID18839357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:26746275..27097318hg38UCSC Ensembl
Outerchr9:26743024..27123262hg38UCSC Ensembl
Innerchr9:26746273..27097316hg19UCSC Ensembl
Outerchr9:26743022..27123260hg19UCSC Ensembl
Innerchr9:26736273..27087316hg18UCSC Ensembl
Outerchr9:26733022..27113260hg18UCSC Ensembl
Cytoband9p21.2
Allele length
AssemblyAllele length
hg38380239
hg19380239
hg18380239
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25788716, essv25791282
Samples
Known GenesCAAP1, IFT74, LRRC19, PLAA, TEK
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891647
Frequency
Sample Size3017
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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