A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5506967



Internal ID283698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:77218819..77218891hg38UCSC Ensembl
chr11:76929864..76929936hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17047248
Samples
Known GenesGDPD4
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5506967
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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