A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552226



Internal ID16339635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:121010375..121024411hg38UCSC Ensembl
Innerchr10:122769888..122783924hg19UCSC Ensembl
Innerchr10:122759878..122773914hg18UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3814037
hg1914037
hg1814037
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1405n54
Supporting Variantsnssv760278
Samples
Known GenesMIR5694
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552226
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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