A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14377457



Internal ID22265387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:25966890..25966998hg38UCSC Ensembl
chr15:26212037..26212145hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3219653
Supporting Variants
SamplesNA19238
Known GenesLOC100128714
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14377457
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