A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5495437



Internal ID272551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:39081931..39087695hg38UCSC Ensembl
chr11:39103481..39109245hg19UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg385765
hg195765
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17043799
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5495437
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer