A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1289n100



Internal ID20152905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:120506099..120595091hg38UCSC Ensembl
chr11:120376808..120465800hg19UCSC Ensembl
chr11:119882018..119971010hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3888993
hg1988993
hg1888993
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1051115, nsv1054301
Samples
Known GenesGRIK4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1289n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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