A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16977120



Internal ID52138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:170931809..170937621hg38UCSC Ensembl
chr5:170358813..170364625hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg385813
hg195813
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5466164
Supporting Variants
Samples
Known GenesRANBP17
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16977120
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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