A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066293



Internal ID18808824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:59844304..59924573hg38UCSC Ensembl
Innerchr20:58419359..58499628hg19UCSC Ensembl
Innerchr20:57852754..57933023hg18UCSC Ensembl
Cytoband20q13.32
Allele length
AssemblyAllele length
hg3880270
hg1980270
hg1880270
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4335n100
Supporting Variantsnssv3584252
Samples
Known GenesPHACTR3, SYCP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066293
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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