A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16974725



Internal ID50527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:149108298..149109227hg38UCSC Ensembl
chr5:148487861..148488790hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg38930
hg19930
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5560939
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16974725
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000468


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