A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067393



Internal ID21976626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:171473732..171473732hg38UCSC Ensembl
chr5:170900736..170900736hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17572823
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067393
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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