A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6062997



Internal ID21972230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2145283..2145283hg38UCSC Ensembl
chr5:2145397..2145397hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg382954
hg192954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17539530
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6062997
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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