A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18181339



Internal ID20748379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72085001..72131100hg38UCSC Ensembl
chr15:72377342..72423441hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg3846100
hg1946100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504957
Supporting Variants
Samples
Known GenesMYO9A, SENP8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18181339
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00028


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