A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16977117



Internal ID52136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:170882383..170887987hg38UCSC Ensembl
chr5:170309387..170314991hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg385605
hg195605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5466101
Supporting Variants
Samples
Known GenesRANBP17
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16977117
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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