A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1049n100



Internal ID22787136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:5766163..5791118hg38UCSC Ensembl
chr11:5787393..5812348hg19UCSC Ensembl
chr11:5743969..5768924hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3824956
hg1924956
hg1824956
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1049814, nsv1042175, nsv1049309, nsv1046530, nsv1054053, nsv1053727, nsv1040616, nsv1049714
Samples
Known GenesOR52N1, OR52N5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1049n100
Frequency
Sample Size11257
Observed Gain21
Observed Loss415
Observed Complex0
Frequencyn/a


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