A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025833



Internal ID84959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95114154..95114228hg38UCSC Ensembl
chr9:97876436..97876510hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5487558
Supporting Variants
Samples
Known GenesFANCC
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025833
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001093


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