A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550412



Internal ID15991135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:35638239..35642852hg38UCSC Ensembl
Innerchr10:35927167..35931780hg19UCSC Ensembl
Innerchr10:35967173..35971786hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg384614
hg194614
hg184614
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1036n54
Supporting Variantsnssv746848, nssv746847
Samples
Known GenesFZD8, MIR4683
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550412
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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