A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051044



Internal ID18793575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:131448229..131942264hg38UCSC Ensembl
Innerchr10:133246492..133755768hg19UCSC Ensembl
Innerchr10:133136482..133605758hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38494036
hg19509277
hg18469277
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv990n100
Supporting Variantsnssv3513502
Samples
Known GenesFLJ46300, PPP2R2D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051044
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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