A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2803772



Internal ID21249110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:18052990..18053149hg38UCSC Ensembl
chr22:18535756..18535915hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38160
hg19160
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13693261
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2803772
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer