A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202216



Internal ID22351407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:181273125..181288654hg38UCSC Ensembl
chr5:180700126..180715655hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3815530
hg1915530
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7688n152
Supporting Variantsnssv14324148
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202216
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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