A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17025834



Internal ID84960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:95115921..95121567hg38UCSC Ensembl
chr9:97878203..97883849hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg385647
hg195647
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5492544
Supporting Variants
Samples
Known GenesFANCC
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17025834
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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