A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5467731



Internal ID245542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87159780..87159859hg38UCSC Ensembl
chr5:86455597..86455676hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16968755
Samples
Known GenesLOC101929380
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5467731
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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