A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696936



Internal ID15086902
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:25268441..25303640hg38UCSC Ensembl
Innerchr22:25664408..25699607hg19UCSC Ensembl
Innerchr22:23994408..24029607hg18UCSC Ensembl
Innerchr22:23988962..24024161hg17UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3835200
hg1935200
hg1835200
hg1735200
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517205
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696936
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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