A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1016n100



Internal ID20152632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1946041..2043381hg38UCSC Ensembl
chr11:1967271..2064611hg19UCSC Ensembl
chr11:1923847..2021187hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3897341
hg1997341
hg1897341
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1044121, nsv1045282, nsv1040032, nsv1053841
Samples
Known GenesH19, MIR675, MRPL23, MRPL23-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1016n100
Frequency
Sample Size29084
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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