A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6079901



Internal ID21989134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:64362920..64362920hg38UCSC Ensembl
chr5:63658747..63658747hg19UCSC Ensembl
Cytoband5q12.3
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17544373
Samples
Known GenesRNF180
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6079901
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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