A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926276



Internal ID22701503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:60200822..60201042hg38UCSC Ensembl
chr11:59968295..59968515hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38221
hg19221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17351644
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926276
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