A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5465629



Internal ID243488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:135516592..135626055hg38UCSC Ensembl
chr4:136437747..136547210hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38109464
hg19109464
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16957301
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5465629
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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