A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1021n100



Internal ID22787108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4215479..4337814hg38UCSC Ensembl
chr11:4236709..4359044hg19UCSC Ensembl
chr11:4193285..4315620hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38122336
hg19122336
hg18122336
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1053588, nsv1054223, nsv1037926, nsv1038465
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)dgv1021n100
Frequency
Sample Size11257
Observed Gain21
Observed Loss35
Observed Complex0
Frequencyn/a


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