A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25781104



Internal ID19173388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:31954821..31961859hg38UCSC Ensembl
Innerchr13:32528958..32535996hg19UCSC Ensembl
Innerchr13:31426958..31433996hg18UCSC Ensembl
Cytoband13q13.1
Allele length
AssemblyAllele length
hg387039
hg197039
hg187039
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)essv25781104
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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