A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020009



Internal ID19109228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:110584993..110649691hg38UCSC Ensembl
Innerchr5:109920694..109985392hg19UCSC Ensembl
Innerchr5:109948593..110013291hg18UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg3864699
hg1964699
hg1864699
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3647023
Samples
Known GenesTMEM232
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020009
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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