A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6076940



Internal ID21986173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:109597466..109597466hg38UCSC Ensembl
chr4:110518622..110518622hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38107
hg19107
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17540770
Samples
Known GenesCCDC109B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6076940
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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