A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6066657



Internal ID21975890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:3402417..3402417hg38UCSC Ensembl
chr6:3402651..3402651hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17571022
Samples
Known GenesSLC22A23
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6066657
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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