A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586719



Internal ID16374128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:64038541..64048700hg38UCSC Ensembl
Innerchr20:62669894..62680053hg19UCSC Ensembl
Innerchr20:62140338..62150497hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3810160
hg1910160
hg1810160
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7699n54
Supporting Variantsnssv944139
Samples
Known GenesLINC00176, SOX18
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586719
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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