A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035650



Internal ID18778181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3753167..3788015hg38UCSC Ensembl
Innerchr10:3795359..3830207hg19UCSC Ensembl
Innerchr10:3785359..3820207hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3834849
hg1934849
hg1834849
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv661n100
Supporting Variantsnssv3483996
Samples
Known GenesKLF6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035650
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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