A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv753170



Internal ID15700440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87870667..87891002hg38UCSC Ensembl
Innerchr10:89630424..89650759hg19UCSC Ensembl
Innerchr10:89620404..89640739hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg3820336
hg1920336
hg1820336
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551832
Supporting Variants
Samples
Known GenesPTEN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv753170
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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