A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040660



Internal ID19129879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:24083364..24099486hg38UCSC Ensembl
Innerchr10:24372293..24388415hg19UCSC Ensembl
Innerchr10:24412299..24428421hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3816123
hg1916123
hg1816123
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv690n100
Supporting Variantsnssv3512080, nssv3521578
Samples
Known GenesKIAA1217
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040660
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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