A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1009n100



Internal ID22787096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133582768..133769367hg38UCSC Ensembl
chr10:135396272..135506692hg19UCSC Ensembl
chr10:135246262..135356682hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38186600
hg19110421
hg18110421
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1048296, nsv1043996
Samples
Known GenesDUX2, DUX4, DUX4L, DUX4L2, DUX4L3, DUX4L5, DUX4L6, DUX4L7, FRG2B, LOC100653046
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1009n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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