A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5513496



Internal ID290019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:62371990..62374709hg38UCSC Ensembl
chr11:62139462..62142181hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg382720
hg192720
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17046649
Samples
Known GenesASRGL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5513496
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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