A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv583199



Internal ID16370608
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 StatusM
Merged Variants
Supporting Variantsnssv920120
Samples
Known GenesLRP1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv583199
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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