A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv869832



Internal ID16163788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:35357016..35433147hg38UCSC Ensembl
Innerchr17:33684035..33760166hg19UCSC Ensembl
Innerchr17:30708148..30784279hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3876132
hg1976132
hg1876132
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574745
Supporting Variants
Samples
Known GenesSLFN11, SLFN12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv869832
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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