A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14377974



Internal ID22265663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25871686..25871686hg38UCSC Ensembl
chr15:26116833..26116833hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3560440
Supporting Variants
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14377974
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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