A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6073879



Internal ID21983112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177554489..177554489hg38UCSC Ensembl
chr5:176981490..176981490hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563870
Samples
Known GenesFAM193B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6073879
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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