A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv583236



Internal ID16370645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:141752001..141810896hg38UCSC Ensembl
Innerchr2:142509570..142568465hg19UCSC Ensembl
Innerchr2:142226040..142284935hg18UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg3858896
hg1958896
hg1858896
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv920271
Samples
Known GenesLRP1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv583236
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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