A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18180286



Internal ID20747326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:59333855..59351988hg38UCSC Ensembl
chr15:59626054..59644187hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3818134
hg1918134
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6508161
Supporting Variants
Samples
Known GenesMYO1E
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18180286
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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