A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6058176



Internal ID21967410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:218541833..218541833hg38UCSC Ensembl
chr1:218715175..218715175hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17531745
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6058176
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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