A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550669



Internal ID16338078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42230215..42487197hg38UCSC Ensembl
Innerchr10:42725663..42982645hg19UCSC Ensembl
Innerchr10:42045669..42302651hg18UCSC Ensembl
Cytoband10q11.1
Allele length
AssemblyAllele length
hg38256983
hg19256983
hg18256983
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1097n54
Supporting Variantsnssv747287
Samples
Known GenesCCNYL2, LINC00839, LOC441666
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550669
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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