A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791364



Internal ID19169763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20019785..22260455hg38UCSC Ensembl
Innerchr15:20225038..22548406hg19UCSC Ensembl
Innerchr15:18485052..20049770hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382240671
hg192323369
hg181564719
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, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2, REREP3
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=149
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791364
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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