A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6066220



Internal ID21975453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:105879976..105879976hg38UCSC Ensembl
chr6:106327851..106327851hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565045
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6066220
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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