A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6010022



Internal ID21919365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:63852185..63852242hg38UCSC Ensembl
chr6:64562078..64562135hg19UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570843
Samples
Known GenesEYS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6010022
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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