A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522434



Internal ID15103041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:24721953..24749486hg38UCSC Ensembl
Innerchr22:25117920..25145453hg19UCSC Ensembl
Innerchr22:23447920..23475453hg18UCSC Ensembl
Innerchr22:23442474..23470007hg17UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3827534
hg1927534
hg1827534
hg1727534
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705790
Samples
Known GenesPIWIL3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522434
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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