A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5465616



Internal ID243475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:21797482..21797626hg38UCSC Ensembl
chr6:21797713..21797857hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16982255
Samples
Known GenesCASC15
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5465616
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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