A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16961910



Internal ID41908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6350681..6350681hg38UCSC Ensembl
chr5:6350794..6350794hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38181
hg19181
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5535429
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16961910
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002188


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