A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550683



Internal ID15991406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:42298677..42570966hg38UCSC Ensembl
Innerchr10:42794125..43066414hg19UCSC Ensembl
Innerchr10:42114131..42386420hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38272290
hg19272290
hg18272290
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1098n54
Supporting Variantsnssv1173553
SamplesHGDP00764
Known GenesCCNYL2, LINC00839, LOC441666, ZNF37BP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550683
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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