A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5503979



Internal ID280790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76796826..76797045hg38UCSC Ensembl
chr11:76507870..76508089hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg38220
hg19220
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17047224
Samples
Known GenesTSKU
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5503979
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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