A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv583202



Internal ID16370611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:141109879..141164063hg38UCSC Ensembl
Innerchr2:141867448..141921632hg19UCSC Ensembl
Innerchr2:141583918..141638102hg18UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg3854185
hg1954185
hg1854185
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151314
Samples1780854477_A
Known GenesLRP1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv583202
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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