A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16968607



Internal ID46391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:82294535..82294573hg38UCSC Ensembl
chr5:81590354..81590392hg19UCSC Ensembl
Cytoband5q14.2
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5542186
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16968607
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.003903


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