A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25791967



Internal ID19168942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:21138819..22227639hg38UCSC Ensembl
Innerchr15:21344148..22515590hg19UCSC Ensembl
Innerchr15:19608807..20016954hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381088821
hg191171443
hg18408148
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892612
Supporting Variants
Samples
Known GenesCXADRP2, LOC646214, LOC727924, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=30
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25791967
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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