A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1150460



Internal ID15872982
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:57785698..57835085hg38UCSC Ensembl
Innerchr2:58012833..58062220hg19UCSC Ensembl
Innerchr2:57866337..57915724hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3849388
hg1949388
hg1849388
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582095
Supporting Variants
SamplesHGDP00092
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1150460
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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