A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062032



Internal ID19151251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:25268006..25512649hg38UCSC Ensembl
Innerchr22:25663973..25908616hg19UCSC Ensembl
Innerchr22:23993973..24238616hg18UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg38244644
hg19244644
hg18244644
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4547n100
Supporting Variantsnssv3588146, nssv3588145
Samples
Known GenesCRYBB2P1, IGLL3P, LRP5L, MIR6817
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062032
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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