A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545692



Internal ID15986415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:17228358..17331039hg38UCSC Ensembl
Innerchr1:17554853..17657534hg19UCSC Ensembl
Innerchr1:17427440..17530121hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38102682
hg19102682
hg18102682
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv710924
Samples
Known GenesPADI1, PADI3, PADI4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545692
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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