A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5452193



Internal ID230353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:238552909..238564958hg38UCSC Ensembl
chr2:239461550..239473599hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3812050
hg1912050
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16927118
Samples
Known GenesLINC01107
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5452193
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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