A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6065545



Internal ID21974778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:41911491..41911491hg38UCSC Ensembl
chr6:41879229..41879229hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg382918
hg192918
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557841
Samples
Known GenesMED20
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6065545
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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