A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551836



Internal ID16339245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87893318..87893929hg38UCSC Ensembl
Innerchr10:89653075..89653686hg19UCSC Ensembl
Innerchr10:89643055..89643666hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38612
hg19612
hg18612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1333n54
Supporting Variantsnssv753217, nssv753213, nssv753216, nssv753203, nssv753219, nssv753196, nssv753197, nssv753211, nssv753202, nssv753210, nssv753215, nssv753200, nssv753212, nssv753207, nssv753205, nssv753204, nssv753209, nssv753195, nssv753201, nssv753218, nssv753199, nssv753206, nssv753198, nssv753208, nssv753214
Samples
Known GenesPTEN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551836
Frequency
Sample Size17421
Observed Gain0
Observed Loss25
Observed Complex0
Frequencyn/a


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