A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5922761



Internal ID22697986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3869000..3872083hg38UCSC Ensembl
chr11:3890230..3893313hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg383084
hg193084
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357253
Samples
Known GenesSTIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5922761
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