A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5539063



Internal ID314061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:35367633..35367633hg38UCSC Ensembl
chr8:35225151..35225151hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17009535
Samples
Known GenesUNC5D
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5539063
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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