A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076799



Internal ID21986032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:138973582..138973582hg38UCSC Ensembl
chr6:139294719..139294719hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557686
Samples
Known GenesREPS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076799
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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