A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231186



Internal ID20798226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64433301..64470000hg38UCSC Ensembl
chr9:69445719..69482418hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg3836700
hg1936700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449622
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231186
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00183


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