A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1321n100



Internal ID22787408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:135002410..135074876hg38UCSC Ensembl
chr11:134872304..134944770hg19UCSC Ensembl
chr11:134377514..134449982hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3872467
hg1972467
hg1872469
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1050751, nsv1039611, nsv1041763, nsv1049292
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)dgv1321n100
Frequency
Sample Size11257
Observed Gain7
Observed Loss6
Observed Complex0
Frequencyn/a


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