A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3524872



Internal ID22385658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150307031..150307088hg38UCSC Ensembl
chr5:149686594..149686651hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14324324, nssv14324323, nssv14324322
SamplesNA19239, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3524872
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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