A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798054



Internal ID19182880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6673465..6744721hg38UCSC Ensembl
Innerchr9:6673465..6744721hg19UCSC Ensembl
Innerchr9:6663465..6734721hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3871257
hg1971257
hg1871257
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891542
Supporting Variants
Samples
Known GenesKDM4C
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=22
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798054
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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