A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25787782



Internal ID18826303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:35678658..35835415hg38UCSC Ensembl
Innerchr6:35646435..35803192hg19UCSC Ensembl
Innerchr6:35754413..35911170hg18UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38156758
hg19156758
hg18156758
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 Human OmniExpress
CommentsNumber of probes=32
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25787782
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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