A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1299n100



Internal ID20152915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131833130..131874253hg38UCSC Ensembl
chr11:131703024..131744147hg19UCSC Ensembl
chr11:131208234..131249357hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3841124
hg1941124
hg1841124
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1053213, nsv1041652
Samples
Known GenesNTM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1299n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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