A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528419



Internal ID22397807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:54337365..54337468hg38UCSC Ensembl
chr17:52414726..52414829hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3596n152
Supporting Variantsnssv14391325, nssv14385882
SamplesHG00512, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528419
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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