A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14381328



Internal ID22141346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26194775..26194826hg38UCSC Ensembl
chr15:26439922..26439973hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3527324
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14381328
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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