A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551837



Internal ID15992560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87947508..88018031hg38UCSC Ensembl
Innerchr10:89707265..89777788hg19UCSC Ensembl
Innerchr10:89697245..89767768hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3870524
hg1970524
hg1870524
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv753220
Samples
Known GenesPTEN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551837
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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