A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552752



Internal ID16340161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133761832..133786996hg38UCSC Ensembl
Innerchr10:135499157..135524321hg19UCSC Ensembl
Innerchr10:135349147..135374311hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3825165
hg1925165
hg1825165
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv763027
Samples
Known GenesDUX4L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552752
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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