A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586560



Internal ID16373969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63217271..63264557hg38UCSC Ensembl
Innerchr20:61848623..61895909hg19UCSC Ensembl
Innerchr20:61319068..61366354hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3847287
hg1947287
hg1847287
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7665n54
Supporting Variantsnssv1150966, nssv1150965
SamplesHGDP00892, HGDP00451
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)nsv586560
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer