A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526708



Internal ID22396091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:90486046..90489124hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg383079
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14308156, nssv14308157
SamplesNA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526708
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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