A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6068442



Internal ID21977675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87445439..87445439hg38UCSC Ensembl
chr5:86741256..86741256hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555739
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6068442
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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