A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25785999



Internal ID19174370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:58510765..58524114hg38UCSC Ensembl
Innerchr2:58737900..58751249hg19UCSC Ensembl
Innerchr2:58591404..58604753hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3813350
hg1913350
hg1813350
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892548
Supporting Variants
Samples
Known GenesLINC01122
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=5
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25785999
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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