A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797407



Internal ID18834680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29891931..29925417hg38UCSC Ensembl
Innerchr6:29859708..29893194hg19UCSC Ensembl
Innerchr6:29967687..30001173hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3833487
hg1933487
hg1833487
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3890806
Supporting Variants
Samples
Known GenesHCG4B
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=10
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797407
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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