A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv935338



Internal ID16229294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:642066..648070hg38UCSC Ensembl
Innerchr20:622710..628714hg19UCSC Ensembl
Innerchr20:570710..576714hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg386005
hg196005
hg186005
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv585190
Supporting Variants
Samples
Known GenesSRXN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv935338
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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