A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25797384



Internal ID19159558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:159819916..159887281hg38UCSC Ensembl
Innerchr2:160676427..160743792hg19UCSC Ensembl
Innerchr2:160384673..160452038hg18UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg3867366
hg1967366
hg1867366
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893504
Supporting Variants
Samples
Known GenesLY75, LY75-CD302
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
CommentsNumber of probes=19
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25797384
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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