A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25800289



Internal ID18820660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31903708..31908870hg38UCSC Ensembl
Innerchr6:31871485..31876647hg19UCSC Ensembl
Innerchr6:31979464..31984626hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg385163
hg195163
hg185163
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 HumanHap 610
CommentsNumber of probes=6
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25800289
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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