A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6063291



Internal ID21972524
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:7145768..7145768hg38UCSC Ensembl
chr6:7146001..7146001hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568702
Samples
Known GenesRREB1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6063291
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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