A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780523



Internal ID19174179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133066817..133080285hg38UCSC Ensembl
Innerchr9:135942204..135955672hg19UCSC Ensembl
Innerchr9:134932025..134945493hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3813469
hg1913469
hg1813469
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891731
Supporting Variants
Samples
Known GenesCEL
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780523
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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