A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5463005



Internal ID240923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:105635474..105642881hg38UCSC Ensembl
chr6:106083349..106090756hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg387408
hg197408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16988641
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5463005
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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