A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16967878



Internal ID45906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:58340192..58340243hg38UCSC Ensembl
chr5:57636019..57636070hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5410944
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16967878
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002654


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