A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6072232



Internal ID21981465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55865579..55865579hg38UCSC Ensembl
chr4:56731745..56731745hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17548008
Samples
Known GenesEXOC1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6072232
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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