A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040332



Internal ID18782863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26861..198621hg38UCSC Ensembl
Innerchr10:72797..244561hg19UCSC Ensembl
Innerchr10:62797..234561hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38171761
hg19171765
hg18171765
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv649n100
Supporting Variantsnssv3488237
Samples
Known GenesTUBB8, ZMYND11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040332
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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