A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046267



Internal ID18788798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:74472784..74535121hg38UCSC Ensembl
Innerchr10:76232542..76294879hg19UCSC Ensembl
Innerchr10:75902548..75964885hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg3862338
hg1962338
hg1862338
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3706107
Samples
Known GenesADK
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046267
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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