A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550415



Internal ID15991138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:35639965..35642290hg38UCSC Ensembl
Innerchr10:35928893..35931218hg19UCSC Ensembl
Innerchr10:35968899..35971224hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg382326
hg192326
hg182326
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv746851
Samples
Known GenesFZD8, MIR4683
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550415
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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