A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525589



Internal ID22394967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178609627..178609853hg38UCSC Ensembl
chr5:178036628..178036854hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38227
hg19227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14323322, nssv14323323
SamplesHG00512, HG00514
Known GenesCLK4
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525589
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer