A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv942121



Internal ID16236077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62327333..62411193hg38UCSC Ensembl
Innerchr20:60902389..60986249hg19UCSC Ensembl
Innerchr20:60335784..60419644hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3883861
hg1983861
hg1883861
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv586495
Supporting Variants
Samples
Known GenesCABLES2, LAMA5, MIR4758, RBBP8NL, RPS21
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv942121
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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