A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5505213



Internal ID281995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:75326942..75327824hg38UCSC Ensembl
chr11:75037986..75038868hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38883
hg19883
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17047208
Samples
Known GenesARRB1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5505213
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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