A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16968587



Internal ID46379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:82053746..82107592hg38UCSC Ensembl
chr5:81349565..81403411hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg3853847
hg1953847
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5466864
Supporting Variants
Samples
Known GenesATG10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16968587
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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