A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574741



Internal ID16015464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:35225256..35500115hg38UCSC Ensembl
Innerchr17:33552275..33827134hg19UCSC Ensembl
Innerchr17:30576388..30851247hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38274860
hg19274860
hg18274860
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv869827
Samples
Known GenesSLFN11, SLFN12, SLFN12L, SLFN13, SLFN5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574741
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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