A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18174582



Internal ID20741622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:111366287..111366669hg38UCSC Ensembl
chr9:114128567..114128949hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg38383
hg19383
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438027
Supporting Variants
Samples
Known GenesKIAA0368
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18174582
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0006


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