A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5443267



Internal ID221668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:155215335..155274292hg38UCSC Ensembl
chr2:156071847..156130804hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg3858958
hg1958958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16920105
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5443267
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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