A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16979781



Internal ID53901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:179849006..179849842hg38UCSC Ensembl
chr5:179276006..179276842hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38837
hg19837
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5470911
Supporting Variants
Samples
Known GenesC5orf45
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16979781
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.005003


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