A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18197019



Internal ID20764059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35665353..35681349hg38UCSC Ensembl
chr9:35665350..35681346hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3815997
hg1915997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6443899
Supporting Variants
Samples
Known GenesCA9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18197019
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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