A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047868



Internal ID18790399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26861..213063hg38UCSC Ensembl
Innerchr10:72797..259003hg19UCSC Ensembl
Innerchr10:62797..249003hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38186203
hg19186207
hg18186207
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv649n100
Supporting Variantsnssv3496342
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)nsv1047868
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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