A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16975451



Internal ID51027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:142014763..142060495hg38UCSC Ensembl
chr5:141394328..141440060hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3845733
hg1945733
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5556237
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16975451
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.019045


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