A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063215



Internal ID19152434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:27161078..27185291hg38UCSC Ensembl
Innerchr22:27557040..27581253hg19UCSC Ensembl
Innerchr22:25887040..25911253hg18UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg3824214
hg1924214
hg1824214
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3600787
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063215
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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