A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5507864



Internal ID284572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:121637700..121643000hg38UCSC Ensembl
chr11:121508409..121513709hg19UCSC Ensembl
Cytoband11q24.1
Allele length
AssemblyAllele length
hg385301
hg195301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17051468
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5507864
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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