A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6050437



Internal ID21959670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158605736..158605736hg38UCSC Ensembl
chr1:158575526..158575526hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38747
hg19747
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17522334
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6050437
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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