A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589142



Internal ID16376551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:47315065..47352800hg38UCSC Ensembl
Innerchr22:47710815..47748550hg19UCSC Ensembl
Innerchr22:46089479..46127214hg18UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3837736
hg1937736
hg1837736
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152200, nssv1152199
SamplesHGDP00650, HGDP00623
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589142
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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