A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510540



Internal ID20883860
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 StatusM
Merged Variants
Supporting Variantsnssv18178505
Samples
Known GenesLOC642423, PDE8A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510540
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer