A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2805031



Internal ID21250369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:44889983..44890032hg38UCSC Ensembl
chr22:45285863..45285912hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13682924
Samples
Known GenesPHF21B
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2805031
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