A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6070455



Internal ID21979688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37616033..37616033hg38UCSC Ensembl
chr4:37617655..37617655hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38296
hg19296
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17555525
Samples
Known GenesRELL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6070455
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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