A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16977478



Internal ID52383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:161632470..161632470hg38UCSC Ensembl
chr5:161059476..161059476hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg381
hg191
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563998
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16977478
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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