A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6079264



Internal ID21988497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:138079554..138079554hg38UCSC Ensembl
chr5:137415243..137415243hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17539195
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6079264
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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