A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553338



Internal ID16340747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5768038..5788000hg38UCSC Ensembl
Innerchr11:5789268..5809230hg19UCSC Ensembl
Innerchr11:5745844..5765806hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3819963
hg1919963
hg1819963
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1620n54
Supporting Variantsnssv766281, nssv766273, nssv766277, nssv766279, nssv766270, nssv766274, nssv766269, nssv766275, nssv766278, nssv766280, nssv766272, nssv766282, nssv766276, nssv766271, nssv766268
Samples
Known GenesOR52N1, OR52N5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553338
Frequency
Sample Size17421
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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