A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14342359



Internal ID22128151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:65594095..65594515hg38UCSC Ensembl
chr8:66506330..66506750hg19UCSC Ensembl
Cytoband8q13.1
Allele length
AssemblyAllele length
hg38421
hg19421
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3229719
Supporting Variants
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14342359
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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