A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3142n100



Internal ID22789229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35344137..35442187hg38UCSC Ensembl
chr17:33671156..33769206hg19UCSC Ensembl
chr17:30695269..30793319hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3898051
hg1998051
hg1898051
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1062593, nsv1066376, nsv1061872, nsv1056952, nsv1065765, nsv1067402, nsv1062610, nsv1066569, nsv1064831, nsv1055525
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)dgv3142n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss58
Observed Complex0
Frequencyn/a


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