A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061815



Internal ID19151034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62436472..62557434hg38UCSC Ensembl
Innerchr20:61011528..61154641hg19UCSC Ensembl
Innerchr20:60444923..60565086hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38120963
hg19143114
hg18120164
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4344n100
Supporting Variantsnssv3584465, nssv3584467, nssv3584466
Samples
Known GenesC20orf166, C20orf166-AS1, GATA5, MIR1-1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061815
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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