A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586561



Internal ID16373970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63217271..63264568hg38UCSC Ensembl
Innerchr20:61848623..61895920hg19UCSC Ensembl
Innerchr20:61319068..61366365hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3847298
hg1947298
hg1847298
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7665n54
Supporting Variantsnssv1150967
Samples1780862585_A
Known GenesBIRC7, FLJ16779, MIR3196, NKAIN4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586561
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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