A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189263



Internal ID20756303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59225650..59407349hg38UCSC Ensembl
chr15:59517849..59699548hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38181700
hg19181700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503464
Supporting Variants
Samples
Known GenesMYO1E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189263
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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