A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6058973



Internal ID21968206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:89802082..89802082hg38UCSC Ensembl
chr1:90267641..90267641hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17520352
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6058973
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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