A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5498898



Internal ID275879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:35208603..35209338hg38UCSC Ensembl
chr11:35230150..35230885hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38736
hg19736
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044205
Samples
Known GenesCD44
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5498898
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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