A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050216



Internal ID21959450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:222814970..222814970hg38UCSC Ensembl
chr1:222988312..222988312hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17530329
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050216
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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