A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780583



Internal ID19178240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:31954821..31961151hg38UCSC Ensembl
Innerchr13:32528958..32535288hg19UCSC Ensembl
Innerchr13:31426958..31433288hg18UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg386331
hg196331
hg186331
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892323
Supporting Variants
Samples
Known GenesEEF1DP3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780583
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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