A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035278



Internal ID18777809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87869516..87881536hg38UCSC Ensembl
Innerchr10:89629273..89641293hg19UCSC Ensembl
Innerchr10:89619253..89631273hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3812021
hg1912021
hg1812021
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3518265, nssv3505869
Samples
Known GenesPTEN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035278
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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