A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5443826



Internal ID222213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:201649160..201654261hg38UCSC Ensembl
chr2:202513883..202518984hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg385102
hg195102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16923720
Samples
Known GenesMPP4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5443826
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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