A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6071030



Internal ID21980263
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:89875544..89875544hg38UCSC Ensembl
chr5:89171361..89171361hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546438
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6071030
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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