A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5443876



Internal ID222261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:85382525..85446084hg38UCSC Ensembl
chr3:85431675..85495234hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3863560
hg1963560
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16936323
Samples
Known GenesCADM2, MIR5688
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5443876
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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