A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv920063



Internal ID15867333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:131319806..131477413hg38UCSC Ensembl
Innerchr2:132077379..132234986hg19UCSC Ensembl
Innerchr2:131793849..131951456hg18UCSC Ensembl
Cytoband2q21.1
Allele length
AssemblyAllele length
hg38157608
hg19157608
hg18157608
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv583142
Supporting Variants
Samples
Known GenesLINC01120, LOC401010, RNU6-81P, TUBA3D, WTH3DI
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv920063
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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