A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044775



Internal ID18787306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26861..204722hg38UCSC Ensembl
Innerchr10:72797..250662hg19UCSC Ensembl
Innerchr10:62797..240662hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38177862
hg19177866
hg18177866
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv649n100
Supporting Variantsnssv3493402
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)nsv1044775
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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