A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv979n100



Internal ID22787066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121001578..121031196hg38UCSC Ensembl
chr10:122761091..122790709hg19UCSC Ensembl
chr10:122751081..122780699hg18UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg3829619
hg1929619
hg1829619
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043862, nsv1041174, nsv1053554
Samples
Known GenesMIR5694
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv979n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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