A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6055162



Internal ID21964395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:78449483..78449483hg38UCSC Ensembl
chr1:78915168..78915168hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17520955
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6055162
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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