A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921801



Internal ID22697025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:22688191..22688367hg38UCSC Ensembl
chr11:22709737..22709913hg19UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38177
hg19177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357149
Samples
Known GenesGAS2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5921801
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