A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17046649



Internal ID98912
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 StatusS
Merged Variantsnsv5513496
Supporting Variants
Samples
Known GenesASRGL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17046649
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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