A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv717745



Internal ID16011701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:79040725..79092119hg38UCSC Ensembl
Innerchr1:79506410..79557804hg19UCSC Ensembl
Innerchr1:79278998..79330392hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3851395
hg1951395
hg1851395
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv546630
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv717745
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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