A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189317



Internal ID20756357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:71972502..71976081hg38UCSC Ensembl
chr15:72264843..72268422hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg383580
hg193580
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6515151
Supporting Variants
Samples
Known GenesMYO9A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189317
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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