A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550008



Internal ID16337417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14948370..15028616hg38UCSC Ensembl
Innerchr10:14990369..15070615hg19UCSC Ensembl
Innerchr10:15030375..15110621hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3880247
hg1980247
hg1880247
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv962n54
Supporting Variantsnssv744091
Samples
Known GenesDCLRE1C, MEIG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550008
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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