A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv583238



Internal ID16370647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:141888794..141981552hg38UCSC Ensembl
Innerchr2:142646363..142739121hg19UCSC Ensembl
Innerchr2:142362833..142455591hg18UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg3892759
hg1992759
hg1892759
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv920272
Samples
Known GenesLRP1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv583238
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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