A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6052070



Internal ID21961303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:371686..371686hg38UCSC Ensembl
chr5:180874205..180874205hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17536302
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6052070
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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