A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv737465



Internal ID16031421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:228276547..228341905hg38UCSC Ensembl
Innerchr1:228464248..228529606hg19UCSC Ensembl
Innerchr1:226530871..226596229hg18UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg3865359
hg1965359
hg1865359
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549293
Supporting Variants
Samples
Known GenesOBSCN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv737465
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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