A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14378893



Internal ID22195032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65805555..65811314hg38UCSC Ensembl
chr15:66097893..66103652hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg385760
hg195760
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3529829
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14378893
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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