A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18185074



Internal ID20752114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62723399..62892082hg38UCSC Ensembl
chr15:63015598..63184281hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38168684
hg19168684
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6501354
Supporting Variants
Samples
Known GenesMIR190A, TLN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18185074
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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