A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5466864



Internal ID244691
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 StatusM
Merged Variants
Supporting Variantsnssv16968587
Samples
Known GenesATG10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5466864
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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