A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054082



Internal ID18796613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:131352375..131844996hg38UCSC Ensembl
Innerchr10:133150638..133677331hg19UCSC Ensembl
Innerchr10:133040628..133527321hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38492622
hg19526694
hg18486694
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv990n100
Supporting Variantsnssv3516491
Samples
Known GenesFLJ46300
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054082
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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