A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552539



Internal ID15993262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133061918..133103793hg38UCSC Ensembl
Innerchr10:134875422..134917297hg19UCSC Ensembl
Innerchr10:134725412..134767287hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3841876
hg1941876
hg1841876
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv761980
Samples
Known GenesGPR123
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552539
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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