A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6081419



Internal ID21990652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:71553196..71553196hg38UCSC Ensembl
chr13:72127328..72127328hg19UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17605774
Samples
Known GenesDACH1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6081419
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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