A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25790097



Internal ID19174620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:18450119..18782350hg38UCSC Ensembl
Innerchr13:19024259..19356490hg19UCSC Ensembl
Innerchr13:17922259..18254490hg18UCSC Ensembl
Cytoband13q11
Allele length
AssemblyAllele length
hg38332232
hg19332232
hg18332232
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892293
Supporting Variants
Samples
Known GenesLINC00417
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=46
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25790097
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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