A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550006



Internal ID15990729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14948370..15018277hg38UCSC Ensembl
Innerchr10:14990369..15060276hg19UCSC Ensembl
Innerchr10:15030375..15100282hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3869908
hg1969908
hg1869908
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv963n54
Supporting Variantsnssv744083
Samples
Known GenesDCLRE1C, MEIG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550006
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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