A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049921



Internal ID19139140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5761683..5787897hg38UCSC Ensembl
Innerchr11:5782913..5809127hg19UCSC Ensembl
Innerchr11:5739489..5765703hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3826215
hg1926215
hg1826215
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1044n100
Supporting Variantsnssv3518475
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)nsv1049921
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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