A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067402



Internal ID19156621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:35357088..35442187hg38UCSC Ensembl
Innerchr17:33684107..33769206hg19UCSC Ensembl
Innerchr17:30708220..30793319hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3885100
hg1985100
hg1885100
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3142n100
Supporting Variantsnssv3561114
Samples
Known GenesSLFN11, SLFN12, SLFN13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067402
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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