A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066176



Internal ID19155395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62448564..62567701hg38UCSC Ensembl
Innerchr20:61023620..61164908hg19UCSC Ensembl
Innerchr20:60457015..60575353hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38119138
hg19141289
hg18118339
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4344n100
Supporting Variantsnssv3584495, nssv3584499, nssv3584501, nssv3584500, nssv3584496, nssv3584498, nssv3584497
Samples
Known GenesC20orf166, C20orf166-AS1, GATA5, MIR1-1, MIR133A2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066176
Frequency
Sample Size11257
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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