A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5495038



Internal ID272162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:44608000..44610789hg38UCSC Ensembl
chr11:44629550..44632339hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg382790
hg192790
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17046134
Samples
Known GenesCD82
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5495038
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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