A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6041586



Internal ID21950919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153015286..153015286hg38UCSC Ensembl
chr1:152987762..152987762hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38533
hg19533
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17532947
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6041586
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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