A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5463335



Internal ID241242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:111258006..111260433hg38UCSC Ensembl
chr6:111579209..111581636hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg382428
hg192428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16988749
Samples
Known GenesKIAA1919
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5463335
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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