A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5914534



Internal ID22689751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:33665347..33665415hg38UCSC Ensembl
chr11:33686893..33686961hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351040
Samples
Known GenesKIAA1549L
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5914534
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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