A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6486633



Internal ID21144186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98972679..99325349hg38UCSC Ensembl
chr13:99624933..99977603hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38352671
hg19352671
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18182475
Samples
Known GenesDOCK9, DOCK9-AS2, GPR18, GPR183, MIR548AN, UBAC2, UBAC2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6486633
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