A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545286



Internal ID16332695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:6962690..6963271hg38UCSC Ensembl
Innerchr1:7022750..7023331hg19UCSC Ensembl
Innerchr1:6945337..6945918hg18UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg38582
hg19582
hg18582
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv84n54
Supporting Variantsnssv709436
Samples
Known GenesCAMTA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545286
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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