A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047359



Internal ID18789890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:97546744..97609256hg38UCSC Ensembl
Innerchr10:99306501..99369013hg19UCSC Ensembl
Innerchr10:99296491..99359003hg18UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg3862513
hg1962513
hg1862513
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3518533
Samples
Known GenesANKRD2, C10orf62, HOGA1, MIR5692C2, UBTD1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047359
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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