A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6055328



Internal ID21964561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:101182954..101182954hg38UCSC Ensembl
chr1:101648510..101648510hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17520413
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6055328
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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