A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6061026



Internal ID21970259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:54348073..54348073hg38UCSC Ensembl
chr4:55214240..55214240hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17544608
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6061026
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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