A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5463088



Internal ID241003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35464489..35464986hg38UCSC Ensembl
chr6:35432266..35432763hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38498
hg19498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16983600
Samples
Known GenesFANCE
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5463088
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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