A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6045880



Internal ID21955138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:213791000..213791000hg38UCSC Ensembl
chr1:213964343..213964343hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg38109
hg19109
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17536923
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6045880
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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