A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545277



Internal ID16332686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:6962639..6963127hg38UCSC Ensembl
Innerchr1:7022699..7023187hg19UCSC Ensembl
Innerchr1:6945286..6945774hg18UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg38489
hg19489
hg18489
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv84n54
Supporting Variantsnssv709222
Samples
Known GenesCAMTA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545277
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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