A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25792782



Internal ID18830032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31489965..31504943hg38UCSC Ensembl
Innerchr6:31457742..31472720hg19UCSC Ensembl
Innerchr6:31565721..31580699hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3814979
hg1914979
hg1814979
Variant TypeCNV gain
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890821
Supporting Variants
Samples
Known GenesMICB
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=25
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25792782
Frequency
Sample Size3017
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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