A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5511963



Internal ID288531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:10778399..10778470hg38UCSC Ensembl
chr11:10799946..10800017hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17043293
Samples
Known GenesCTR9
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5511963
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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