A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18182603



Internal ID20749643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35415956..35418080hg38UCSC Ensembl
chr9:35415953..35418077hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg382125
hg192125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448553
Supporting Variants
Samples
Known GenesATP8B5P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18182603
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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