A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5532n54



Internal ID22773427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:35357016..35439928hg38UCSC Ensembl
chr17:33684035..33766947hg19UCSC Ensembl
chr17:30708148..30791060hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3882913
hg1982913
hg1882913
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv574745, nsv574751, nsv574746, nsv574748, nsv574747, nsv574750
Samples1780854176_A, HGDP00161
Known GenesSLFN11, SLFN12, SLFN13
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5532n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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