A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17735393



Internal ID159059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77866261..77870649hg38UCSC Ensembl
chr5:77162085..77166473hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg384389
hg194389
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5555328
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17735393
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000156


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