A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5442288



Internal ID220718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:156218123..156223198hg38UCSC Ensembl
chr2:157074635..157079710hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg385076
hg195076
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16920627
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5442288
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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