A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526209



Internal ID20899570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:81605096..81723001hg38UCSC Ensembl
chr17:79572122..79690031hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38117906
hg19117910
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178276
Samples
Known GenesARL16, CCDC137, HGS, MIR6786, MRPL12, NPLOC4, OXLD1, PDE6G, SLC25A10, TSPAN10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526209
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