A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5472277



Internal ID249993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:67374723..67478420hg38UCSC Ensembl
chr4:68240441..68344138hg19UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg38103698
hg19103698
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16949479
Samples
Known GenesCENPC
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5472277
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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