A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056657



Internal ID18799188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:16755628..16995464hg38UCSC Ensembl
Innerchr20:16736273..16976109hg19UCSC Ensembl
Innerchr20:16684273..16924109hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38239837
hg19239837
hg18239837
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584639
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056657
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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