A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16977913



Internal ID52674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:181403700..181477493hg38UCSC Ensembl
chr5:180830701..180904494hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3873794
hg1973794
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6140687
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16977913
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000631


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