A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6061738



Internal ID21970971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:116589010..116589010hg38UCSC Ensembl
chr6:116910173..116910173hg19UCSC Ensembl
Cytoband6q22.1
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577221
Samples
Known GenesRWDD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6061738
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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