A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584171



Internal ID16371580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:201999764..202030440hg38UCSC Ensembl
Innerchr2:202864487..202895163hg19UCSC Ensembl
Innerchr2:202572732..202603408hg18UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg3830677
hg1930677
hg1830677
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv930365
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584171
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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