A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5443149



Internal ID221552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:10654398..10654478hg38UCSC Ensembl
chr2:10794524..10794604hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16909440
Samples
Known GenesNOL10
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5443149
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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