A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5497650



Internal ID274676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:66874127..66889433hg38UCSC Ensembl
chr11:66641598..66656904hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3815307
hg1915307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17046229
Samples
Known GenesPC
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5497650
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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