A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054986



Internal ID18797517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26861..138027hg38UCSC Ensembl
Innerchr10:72797..183967hg19UCSC Ensembl
Innerchr10:62797..173967hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38111167
hg19111171
hg18111171
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv648n100
Supporting Variantsnssv3484234, nssv3497469, nssv3501343
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)nsv1054986
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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