A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059142



Internal ID18801673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:63731978..63798885hg38UCSC Ensembl
Innerchr20:62363330..62430238hg19UCSC Ensembl
Innerchr20:61833774..61900682hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg3866908
hg1966909
hg1866909
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3731551
Samples
Known GenesLIME1, SLC2A4RG, ZBTB46, ZGPAT
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059142
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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