A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066569



Internal ID19155788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:35344137..35431547hg38UCSC Ensembl
Innerchr17:33671156..33758566hg19UCSC Ensembl
Innerchr17:30695269..30782679hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3887411
hg1987411
hg1887411
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3142n100
Supporting Variantsnssv3561069
Samples
Known GenesSLFN11, SLFN12
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066569
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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