A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5441099



Internal ID219583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:180604581..180613980hg38UCSC Ensembl
chr2:181469308..181478707hg19UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg389400
hg199400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16922412
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5441099
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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