A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16973328



Internal ID49599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:119668403..119689807hg38UCSC Ensembl
chr5:119004098..119025502hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3821405
hg1921405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5456532
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16973328
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001405


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