A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14379215



Internal ID22281289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71858185..71863497hg38UCSC Ensembl
chr15:72150526..72155838hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg385313
hg195313
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3211534
Supporting Variants
SamplesNA19239
Known GenesMYO9A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14379215
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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