A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229002



Internal ID20796042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95001501..95007000hg38UCSC Ensembl
chr9:97763783..97769282hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg385500
hg195500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6449970
Supporting Variants
Samples
Known GenesC9orf3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229002
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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