A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18175069



Internal ID20742109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:114616485..114618131hg38UCSC Ensembl
chr9:117378765..117380411hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg381647
hg191647
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6453665
Supporting Variants
Samples
Known GenesC9orf91
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18175069
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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