A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16954890



Internal ID37242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:109615573..109623479hg38UCSC Ensembl
chr4:110536729..110544635hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg387907
hg197907
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5455676
Supporting Variants
Samples
Known GenesCCDC109B
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16954890
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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