A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6070622



Internal ID21979855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:55569962..55569962hg38UCSC Ensembl
chr5:54865790..54865790hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17546640
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6070622
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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