A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv920120



Internal ID16214076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:140793781..140825637hg38UCSC Ensembl
Innerchr2:141551350..141583206hg19UCSC Ensembl
Innerchr2:141267820..141299676hg18UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg3831857
hg1931857
hg1831857
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv583199
Supporting Variants
Samples
Known GenesLRP1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv920120
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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