A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16975367



Internal ID50966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:165562773..165568690hg38UCSC Ensembl
chr5:164989778..164995695hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg385918
hg195918
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467633
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16975367
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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