A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798094



Internal ID18813759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:29900276..29928643hg38UCSC Ensembl
Innerchr6:29868053..29896420hg19UCSC Ensembl
Innerchr6:29976032..30004399hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3828368
hg1928368
hg1828368
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=8
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798094
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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