A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3211534



Internal ID22359062
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14386091, nssv14379215
SamplesNA19239, NA19240
Known GenesMYO9A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3211534
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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