A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062308



Internal ID19151527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:26100352..26217295hg38UCSC Ensembl
Innerchr20:26080988..26197931hg19UCSC Ensembl
Innerchr20:26028988..26145931hg18UCSC Ensembl
Cytoband20p11.1
Allele length
AssemblyAllele length
hg38116944
hg19116944
hg18116944
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584687
Samples
Known GenesLOC284801, MIR663A, NCOR1P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062308
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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