A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5500538



Internal ID277471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5561887..5563392hg38UCSC Ensembl
chr11:5583117..5584622hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381506
hg191506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17043175
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5500538
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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