A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5507905



Internal ID284610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:32803447..32812875hg38UCSC Ensembl
chr11:32824993..32834421hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg389429
hg199429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17043092
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5507905
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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