A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892393



Internal ID19183213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:74319884..74447319hg38UCSC Ensembl
Outerchr13:74319884..74447319hg38UCSC Ensembl
Innerchr13:74894021..75021456hg19UCSC Ensembl
Outerchr13:74894021..75021456hg19UCSC Ensembl
Innerchr13:73792022..73919457hg18UCSC Ensembl
Outerchr13:73792022..73919457hg18UCSC Ensembl
Cytoband13q22.1
Allele length
AssemblyAllele length
hg38127436
hg19127436
hg18127436
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25792764
Samples
Known GenesLINC00381
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892393
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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