A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5512313



Internal ID288869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95471233..95473614hg38UCSC Ensembl
chr11:95204397..95206778hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg382382
hg192382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17050084
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5512313
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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