A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581711



Internal ID16369120
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 StatusM
Merged Variantsdgv6841n54
Supporting Variantsnssv1150435
SamplesHGDP01373
Known GenesLINC01121
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581711
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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