A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525674



Internal ID22395052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:170040686..170040945hg38UCSC Ensembl
chr5:169467690..169467949hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38260
hg19260
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14323802
SamplesNA19239
Known GenesDOCK2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525674
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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