A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574746



Internal ID16362155
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 StatusM
Merged Variantsdgv5532n54
Supporting Variantsnssv869836, nssv869835
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)nsv574746
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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