A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460459



Internal ID238441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:170073785..170073864hg38UCSC Ensembl
chr6:170389009..170389088hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16990408
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460459
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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