A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039703



Internal ID19128922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4785439..4889142hg38UCSC Ensembl
Innerchr11:4806669..4910372hg19UCSC Ensembl
Innerchr11:4763245..4866948hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38103704
hg19103704
hg18103704
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1026n100
Supporting Variantsnssv3510980, nssv3508807
Samples
Known GenesOR51F2, OR51S1, OR51T1, OR52R1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039703
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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