A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6043919



Internal ID21953210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:223478905..223478905hg38UCSC Ensembl
chr1:223652247..223652247hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17530522
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6043919
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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