A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5498832



Internal ID275816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:64274169..64274599hg38UCSC Ensembl
chr11:64041641..64042071hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg38431
hg19431
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17046708
Samples
Known GenesBAD
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5498832
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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