A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5509901



Internal ID286537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:72549124..72550529hg38UCSC Ensembl
chr11:72260168..72261573hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg381406
hg191406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17047137
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5509901
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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