A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5532113



Internal ID308043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:35471018..35471163hg38UCSC Ensembl
chr18:33050982..33051127hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38146
hg19146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17717310
Samples
Known GenesINO80C
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5532113
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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