A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5453980



Internal ID232088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10332668..10332811hg38UCSC Ensembl
chr6:10332901..10333044hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38144
hg19144
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16979554
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5453980
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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