A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892694



Internal ID19183514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:54502842..54627341hg38UCSC Ensembl
Outerchr15:54502842..54627341hg38UCSC Ensembl
Innerchr15:54795040..54919539hg19UCSC Ensembl
Outerchr15:54795040..54919539hg19UCSC Ensembl
Innerchr15:52582332..52706831hg18UCSC Ensembl
Outerchr15:52582332..52706831hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38124500
hg19124500
hg18124500
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25791800
Samples
Known GenesUNC13C
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892694
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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