A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151297



Internal ID15874023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:131319806..131540895hg38UCSC Ensembl
Innerchr2:132077379..132298468hg19UCSC Ensembl
Innerchr2:131793849..132014938hg18UCSC Ensembl
Cytoband2q21.1
Allele length
AssemblyAllele length
hg38221090
hg19221090
hg18221090
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv583143
Supporting Variants
SamplesHGDP00460
Known GenesCCDC74A, LINC01120, LOC150776, LOC401010, MIR4784, MZT2A, RNU6-81P, TUBA3D, WTH3DI
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151297
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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