A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5915995



Internal ID22691214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:9302093..9303102hg38UCSC Ensembl
chr11:9323640..9324649hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381010
hg191010
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17360260
Samples
Known GenesTMEM41B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5915995
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