A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012534



Internal ID21921877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:167784654..167784850hg38UCSC Ensembl
chr6:168185334..168185530hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38197
hg19197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563342
Samples
Known GenesC6orf123
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012534
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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