A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5403391



Internal ID182751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:77160303..77160303hg38UCSC Ensembl
chr4:78081456..78081456hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16952401
Samples
Known GenesCCNG2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5403391
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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