A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5506056



Internal ID282811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:12989329..12989412hg38UCSC Ensembl
chr11:13010876..13010959hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17042933
Samples
Known GenesLINC00958
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5506056
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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