A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791775



Internal ID18815871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18450119..18942494hg38UCSC Ensembl
Innerchr13:19024259..19516634hg19UCSC Ensembl
Innerchr13:17922259..18414634hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38492376
hg19492376
hg18492376
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892294
Supporting Variants
Samples
Known GenesANKRD20A9P, LINC00408, LINC00417
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=70
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791775
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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