A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25782337



Internal ID19175774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:13257923..13264566hg38UCSC Ensembl
Innerchr10:13299923..13306566hg19UCSC Ensembl
Innerchr10:13339929..13346572hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg386644
hg196644
hg186644
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891759
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25782337
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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