A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787414



Internal ID18832611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18967770..19048003hg38UCSC Ensembl
Innerchr13:19541910..19622143hg19UCSC Ensembl
Innerchr13:18439910..18520143hg18UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3880234
hg1980234
hg1880234
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892290
Supporting Variants
Samples
Known GenesLINC00442
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=20
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787414
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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