A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055670



Internal ID18798201
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 StatusM
Merged Variantsdgv4347n100
Supporting Variantsnssv3584509
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)nsv1055670
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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