A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035154



Internal ID18777685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87897393..87916728hg38UCSC Ensembl
Innerchr10:89657150..89676485hg19UCSC Ensembl
Innerchr10:89647130..89666465hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3819336
hg1919336
hg1819336
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3503495
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)nsv1035154
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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