A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25796478



Internal ID18830833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31904606..31910655hg38UCSC Ensembl
Innerchr6:31872383..31878432hg19UCSC Ensembl
Innerchr6:31980362..31986411hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg386050
hg196050
hg186050
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890823
Supporting Variants
Samples
Known GenesC2
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25796478
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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