A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18193551



Internal ID20760591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90072067..90093883hg38UCSC Ensembl
chr15:90615299..90637115hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3821817
hg1921817
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6505493
Supporting Variants
Samples
Known GenesIDH2, ZNF710
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18193551
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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