A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16977119



Internal ID52137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:170897393..170898133hg38UCSC Ensembl
chr5:170324397..170325137hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38741
hg19741
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5470402
Supporting Variants
Samples
Known GenesRANBP17
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16977119
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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