A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551545



Internal ID15992268
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:76496115..76505371hg38UCSC Ensembl
Innerchr10:78255873..78265129hg19UCSC Ensembl
Innerchr10:77925879..77935135hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg389257
hg199257
hg189257
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1268n54
Supporting Variantsnssv751726, nssv751725
Samples
Known GenesC10orf11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551545
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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