A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054536



Internal ID18797067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:128923253..129746972hg38UCSC Ensembl
Innerchr10:130721517..131545236hg19UCSC Ensembl
Innerchr10:130611507..131435226hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38823720
hg19823720
hg18823720
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3522653
Samples
Known GenesMGMT
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054536
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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