A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv505n145



Internal ID22813521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67422122..67428559hg38UCSC Ensembl
chr17:65418238..65424675hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg386438
hg196438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3111012, nsv3116866, nsv3115534
Samplessample83, sample116, sample7, sample197
Known GenesPITPNC1
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv505n145
Frequency
Sample Size467
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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