A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663579



Internal ID15400231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:19963748..19995491hg38UCSC Ensembl
Innerchr22:19951271..19983014hg19UCSC Ensembl
Innerchr22:18331271..18363014hg18UCSC Ensembl
Innerchr22:18325825..18357568hg17UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3831744
hg1931744
hg1831744
hg1731744
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517165
Supporting Variants
Samples
Known GenesARVCF, COMT, MIR4761
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv663579
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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