A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066181



Internal ID18808712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:34682373..34725674hg38UCSC Ensembl
Innerchr20:33270177..33313478hg19UCSC Ensembl
Innerchr20:32733838..32777139hg18UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3843302
hg1943302
hg1843302
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3737196
Samples
Known GenesNCOA6, TP53INP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066181
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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