A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1019n100



Internal ID20152635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:3881996..3919496hg38UCSC Ensembl
chr11:3903226..3940726hg19UCSC Ensembl
chr11:3859802..3897302hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3837501
hg1937501
hg1837501
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051904, nsv1050077
Samples
Known GenesSTIM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1019n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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