A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545403



Internal ID15986126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:10649384..10690375hg38UCSC Ensembl
Innerchr1:10709441..10750432hg19UCSC Ensembl
Innerchr1:10632028..10673019hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3840992
hg1940992
hg1840992
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv709926
Samples
Known GenesCASZ1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545403
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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