A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16975894



Internal ID51326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:156798284..156798335hg38UCSC Ensembl
chr5:156225295..156225346hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5405227
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16975894
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002658


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