A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062935



Internal ID19152154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:24949471..25005969hg38UCSC Ensembl
Innerchr22:25345438..25401936hg19UCSC Ensembl
Innerchr22:23675438..23731936hg18UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3856499
hg1956499
hg1856499
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3588058
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)nsv1062935
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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