A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14373976



Internal ID22139116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65151345..65151480hg38UCSC Ensembl
chr15:65443683..65443818hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3225251
Supporting Variants
SamplesHG00513
Known GenesCLPX
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14373976
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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