A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550414



Internal ID15991137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:35638365..35642852hg38UCSC Ensembl
Innerchr10:35927293..35931780hg19UCSC Ensembl
Innerchr10:35967299..35971786hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg384488
hg194488
hg184488
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1036n54
Supporting Variantsnssv746850
Samples
Known GenesFZD8, MIR4683
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550414
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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