A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5442640



Internal ID221061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:159919475..159919629hg38UCSC Ensembl
chr2:160775986..160776140hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38155
hg19155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16921382
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5442640
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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