A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6019166



Internal ID21928509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26937239..27028819hg38UCSC Ensembl
chr6:26905018..26996598hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3891581
hg1991581
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575105
Samples
Known GenesGUSBP2, LINC00240, LOC100270746
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6019166
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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