A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25788882



Internal ID18827715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35703874..35837356hg38UCSC Ensembl
Innerchr6:35671651..35805133hg19UCSC Ensembl
Innerchr6:35779629..35913111hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38133483
hg19133483
hg18133483
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890842
Supporting Variants
Samples
Known GenesARMC12, CLPS, CLPSL1, CLPSL2, FKBP5, LHFPL5, LOC285847, SRPK1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=24
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25788882
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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