A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16972806



Internal ID49236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:117821051..117878584hg38UCSC Ensembl
chr5:117156746..117214279hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3857534
hg1957534
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467251
Supporting Variants
Samples
Known GenesLOC102467224
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16972806
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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