A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5500686



Internal ID277613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:82889984..82890053hg38UCSC Ensembl
chr11:82601026..82601095hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17048406
Samples
Known GenesPRCP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5500686
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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