A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv913928



Internal ID16207884
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:89192287..90239257hg38UCSC Ensembl
Innerchr2:89491775..90278124hg19UCSC Ensembl
Innerchr2:89272890..89915429hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg381046971
hg19786350
hg18642540
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582398
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv913928
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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