A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3584509



Internal ID18536104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:64138667..64324788hg38UCSC Ensembl
Innerchr20:62770020..62956141hg19UCSC Ensembl
Innerchr20:62240464..62426585hg18UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38186122
hg19186122
hg18186122
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055670
Supporting Variants
Samples
Known GenesLINC00266-1, MYT1, PCMTD2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3584509
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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