A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5446727



Internal ID225047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:159147164..159147851hg38UCSC Ensembl
chr2:160003675..160004362hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38688
hg19688
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16926611
Samples
Known GenesTANC1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5446727
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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