A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012308



Internal ID18754841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:167193111..167248071hg38UCSC Ensembl
Innerchr3:166910899..166965859hg19UCSC Ensembl
Innerchr3:168393593..168448553hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3854961
hg1954961
hg1854961
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4982n100
Supporting Variantsnssv3612698
Samples
Known GenesZBBX
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012308
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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