A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497559



Internal ID20870766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:85050560..85053090hg38UCSC Ensembl
chr16:85084166..85086696hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg382531
hg192531
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033081
Samples
Known GenesKIAA0513
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497559
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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