A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv5742n54



Internal ID22773637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:62978029..63155117hg38UCSC Ensembl
chr17:61055390..61232478hg19UCSC Ensembl
chr17:58409122..58586210hg18UCSC Ensembl
Cytoband17q23.2
Allele length
AssemblyAllele length
hg38177089
hg19177089
hg18177089
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv575849, nsv575852
SamplesHGDP00647
Known GenesMIR548W, TANC2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv5742n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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