A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3202191



Internal ID22351390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:14927764..14928352hg38UCSC Ensembl
chr5:14927873..14928461hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg38589
hg19589
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14320341, nssv14320340
SamplesNA19240, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3202191
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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