A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25783040



Internal ID18822990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:2198627..2272512hg38UCSC Ensembl
Innerchr9:2198627..2272512hg19UCSC Ensembl
Innerchr9:2188627..2262512hg18UCSC Ensembl
Cytoband9p24.2
Allele length
AssemblyAllele length
hg3873886
hg1973886
hg1873886
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891521
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=37
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25783040
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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