A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6071788



Internal ID21981021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:170083834..170083834hg38UCSC Ensembl
chr4:171004985..171004985hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg38304
hg19304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17547240
Samples
Known GenesAADAT
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6071788
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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