A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060927



Internal ID19150146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:35357088..35423226hg38UCSC Ensembl
Innerchr17:33684107..33750245hg19UCSC Ensembl
Innerchr17:30708220..30774358hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3866139
hg1966139
hg1866139
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3561074
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)nsv1060927
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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