A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586124



Internal ID16026847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:45722456..45749572hg38UCSC Ensembl
Innerchr20:44351095..44378211hg19UCSC Ensembl
Innerchr20:43784509..43811618hg18UCSC Ensembl
Cytoband20q13.12
Allele length
AssemblyAllele length
hg3827117
hg1927117
hg1827110
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7592n54
Supporting Variantsnssv940855, nssv940856
Samples
Known GenesSPINT4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586124
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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