A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv875896



Internal ID16169852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:67969488..67979576hg38UCSC Ensembl
Innerchr17:65965604..65975692hg19UCSC Ensembl
Innerchr17:63396066..63406154hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3810089
hg1910089
hg1810089
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575916
Supporting Variants
Samples
Known GenesBPTF
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv875896
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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