A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5467781



Internal ID245590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:89136173..89141974hg38UCSC Ensembl
chr6:89845892..89851693hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg385802
hg195802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16985335
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5467781
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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