A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060042



Internal ID19149261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:55130423..55165844hg38UCSC Ensembl
Innerchr20:53746962..53782383hg19UCSC Ensembl
Innerchr20:53180369..53215790hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3835422
hg1935422
hg1835422
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4332n100
Supporting Variantsnssv3584230, nssv3584228, nssv3584227, nssv3584229, nssv3584226
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060042
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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