A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893504



Internal ID19184324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:159819916..159887281hg38UCSC Ensembl
Outerchr2:159819916..159887281hg38UCSC Ensembl
Innerchr2:160676427..160743792hg19UCSC Ensembl
Outerchr2:160676427..160743792hg19UCSC Ensembl
Innerchr2:160384673..160452038hg18UCSC Ensembl
Outerchr2:160384673..160452038hg18UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg3867366
hg1967366
hg1867366
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25797384
Samples
Known GenesLY75, LY75-CD302
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893504
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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