A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045073



Internal ID21954343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:173789779..173789779hg38UCSC Ensembl
chr1:173758917..173758917hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg38595
hg19595
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17523874
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045073
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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