A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv984n100



Internal ID22787071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121673138..121696088hg38UCSC Ensembl
chr10:123432652..123455602hg19UCSC Ensembl
chr10:123422642..123445592hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3822951
hg1922951
hg1822951
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1045804, nsv1054625, nsv1036503
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv984n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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