A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550001



Internal ID15990724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14913179..15028616hg38UCSC Ensembl
Innerchr10:14955178..15070615hg19UCSC Ensembl
Innerchr10:14995184..15110621hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38115438
hg19115438
hg18115438
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv961n54
Supporting Variantsnssv744081, nssv744080
Samples
Known GenesDCLRE1C, MEIG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550001
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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