A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14381007



Internal ID22282379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:79840183..79840239hg38UCSC Ensembl
chr15:80132525..80132581hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3529121
Supporting Variants
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14381007
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer