A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5907884



Internal ID22683094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60442101..60442177hg38UCSC Ensembl
chr11:60209574..60209650hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17349924
Samples
Known GenesMS4A5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5907884
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