A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574747



Internal ID16362156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:35357016..35436659hg38UCSC Ensembl
Innerchr17:33684035..33763678hg19UCSC Ensembl
Innerchr17:30708148..30787791hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3879644
hg1979644
hg1879644
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5532n54
Supporting Variantsnssv869837, nssv869838, nssv869841, nssv869840, nssv869842, nssv869839
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)nsv574747
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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