A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035699



Internal ID19124918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5776371..5791118hg38UCSC Ensembl
Innerchr11:5797601..5812348hg19UCSC Ensembl
Innerchr11:5754177..5768924hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3814748
hg1914748
hg1814748
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1052n100
Supporting Variantsnssv3507725, nssv3708499, nssv3708496, nssv3708498, nssv3708500, nssv3521048, nssv3516473, nssv3708497
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)nsv1035699
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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