A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574745



Internal ID16362154
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 StatusM
Merged Variantsdgv5532n54
Supporting Variantsnssv869832, nssv869834, nssv869831, nssv869830, nssv869833
Samples
Known GenesSLFN11, SLFN12
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574745
Frequency
Sample Size17421
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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