A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv869836



Internal ID16163792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:35357016..35435298hg38UCSC Ensembl
Innerchr17:33684035..33762317hg19UCSC Ensembl
Innerchr17:30708148..30786430hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3878283
hg1978283
hg1878283
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574746
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)nssv869836
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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