A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6074861



Internal ID21984094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:72089841..72089841hg38UCSC Ensembl
chr6:72799544..72799544hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38407
hg19407
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565753
Samples
Known GenesRIMS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6074861
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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