A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892632



Internal ID18836766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:23375712..24546172hg38UCSC Ensembl
Outerchr15:23375712..24546172hg38UCSC Ensembl
Innerchr15:23620859..24791319hg19UCSC Ensembl
Outerchr15:23620859..24791319hg19UCSC Ensembl
Innerchr15:21172300..22342412hg18UCSC Ensembl
Outerchr15:21172300..22342412hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381170461
hg191170461
hg181170113
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25790734
Samples
Known GenesMAGEL2, MIR4508, MKRN3, NDN, PWRN2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892632
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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