A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5503119



Internal ID279961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:34891882..34899608hg38UCSC Ensembl
chr11:34913429..34921155hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg387727
hg197727
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17044173
Samples
Known GenesAPIP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5503119
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