A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5469626



Internal ID247405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99761088..99774986hg38UCSC Ensembl
chr4:100682245..100696143hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg3813899
hg1913899
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16952012
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5469626
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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