A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv942126



Internal ID16236082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62645662..62776055hg38UCSC Ensembl
Innerchr20:61277014..61407407hg19UCSC Ensembl
Innerchr20:60747459..60877852hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38130394
hg19130394
hg18130394
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586503
Supporting Variants
Samples
Known GenesLINC00659, LOC100127888, NTSR1, SLCO4A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv942126
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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