A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150435



Internal ID15879479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:45253003..45314247hg38UCSC Ensembl
Innerchr2:45480142..45541386hg19UCSC Ensembl
Innerchr2:45333646..45394890hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg3861245
hg1961245
hg1861245
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv581711
Supporting Variants
SamplesHGDP01373
Known GenesLINC01121
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150435
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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