A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6063196



Internal ID21972429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:26297110..26297110hg38UCSC Ensembl
chr5:26297219..26297219hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17554523
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6063196
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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