A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6053137



Internal ID21962370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:90838466..90838466hg38UCSC Ensembl
chr1:91304023..91304023hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17529636
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6053137
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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