A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5497600



Internal ID274629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:69139778..69141532hg38UCSC Ensembl
chr11:68907246..68909000hg19UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg381755
hg191755
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17047680
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5497600
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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