A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1130n100



Internal ID22787217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:49705833..50004453hg38UCSC Ensembl
chr11:49727385..50025974hg19UCSC Ensembl
chr11:49683961..49982550hg18UCSC Ensembl
Cytoband11p11.12
Allele length
AssemblyAllele length
hg38298621
hg19298590
hg18298590
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1043841, nsv1035961, nsv1035638, nsv1045103, nsv1037200
Samples
Known GenesLOC440040, OR4C12, OR4C13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1130n100
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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