A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16968436



Internal ID46273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77073101..77073101hg38UCSC Ensembl
chr5:76368926..76368926hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg38218
hg19218
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5412386
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16968436
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.037138


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