A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687409



Internal ID15077375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:22165674..22167132hg38UCSC Ensembl
Innerchr22:22520067..22521525hg19UCSC Ensembl
Innerchr22:20850067..20851525hg18UCSC Ensembl
Innerchr22:20844621..20846079hg17UCSC Ensembl
Cytoband22q11.22
Allele length
AssemblyAllele length
hg381459
hg191459
hg181459
hg171459
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516394
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv687409
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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