A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6043206



Internal ID21889728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10035301..10035301hg38UCSC Ensembl
chr1:10095359..10095359hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17520147
Samples
Known GenesUBE4B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6043206
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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