A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5466483



Internal ID244319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:166267954..166280940hg38UCSC Ensembl
chr6:166681442..166694428hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3812987
hg1912987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16990990
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5466483
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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