A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5460213



Internal ID238205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:64732941..64733702hg38UCSC Ensembl
chr6:65442834..65443595hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg38762
hg19762
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17735552
Samples
Known GenesEYS
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5460213
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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