A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv869828



Internal ID15817098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:35337025..35447140hg38UCSC Ensembl
Innerchr17:33664044..33774159hg19UCSC Ensembl
Innerchr17:30688157..30798272hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38110116
hg19110116
hg18110116
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574743
Supporting Variants
Samples
Known GenesSLFN11, SLFN12, SLFN13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv869828
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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