A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25780904



Internal ID19172242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:41229175..41234906hg38UCSC Ensembl
Innerchr5:41229277..41235008hg19UCSC Ensembl
Innerchr5:41265034..41270765hg18UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg385732
hg195732
hg185732
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3894182
Supporting Variants
Samples
Known GenesC6
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25780904
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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