A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582260



Internal ID16369669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:77709169..77800172hg38UCSC Ensembl
Innerchr2:77936295..78027298hg19UCSC Ensembl
Innerchr2:77789803..77880806hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3891004
hg1991004
hg1891004
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv913437
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582260
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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