A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3529121



Internal ID22398514
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3003n152
Supporting Variantsnssv14387588, nssv14381007, nssv14379417
SamplesNA19238, NA19239, HG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3529121
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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