A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6055532



Internal ID21964765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:60064783..60064783hg38UCSC Ensembl
chr1:60530455..60530455hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17535787
Samples
Known GenesC1orf87
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6055532
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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