A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5440578



Internal ID219078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99027824..99085713hg38UCSC Ensembl
chr3:98746668..98804557hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3857890
hg1957890
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16936839
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5440578
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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