A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051496



Internal ID18794027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34881487..35021379hg38UCSC Ensembl
Innerchr10:35170415..35310307hg19UCSC Ensembl
Innerchr10:35210421..35350313hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38139893
hg19139893
hg18139893
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv705n100
Supporting Variantsnssv3520437
Samples
Known GenesCUL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051496
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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