A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581798



Internal ID16369207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:49287592..49335397hg38UCSC Ensembl
Innerchr2:49514731..49562536hg19UCSC Ensembl
Innerchr2:49368235..49416040hg18UCSC Ensembl
Cytoband2p16.3
Allele length
AssemblyAllele length
hg3847806
hg1947806
hg1847806
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6856n54
Supporting Variantsnssv1150446
SamplesNINDS_72
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581798
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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