A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178505



Internal ID20745545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:85019882..85239365hg38UCSC Ensembl
chr15:85563113..85782596hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg38219484
hg19219484
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6510540
Supporting Variants
Samples
Known GenesLOC642423, PDE8A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178505
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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