A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5450933



Internal ID229126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:241193374..241193662hg38UCSC Ensembl
chr2:242132789..242133077hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16927175
Samples
Known GenesANO7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5450933
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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