A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1084n100



Internal ID22787171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:28384121..28480307hg38UCSC Ensembl
chr11:28405668..28501854hg19UCSC Ensembl
chr11:28362244..28458430hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg3896187
hg1996187
hg1896187
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1037611, nsv1046385, nsv1053906
Samples
Known GenesMIR8068
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1084n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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