A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792352



Internal ID19174938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20065683..21999180hg38UCSC Ensembl
Innerchr15:20270936..22287131hg19UCSC Ensembl
Innerchr15:18530950..19788495hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381933498
hg192016196
hg181257546
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892607
Supporting Variants
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, POTEB, POTEB2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=128
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792352
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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