A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv554894



Internal ID15995617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55603545..55669650hg38UCSC Ensembl
Innerchr11:55371021..55437126hg19UCSC Ensembl
Innerchr11:55127597..55193702hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3866106
hg1966106
hg1866106
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1915n54
Supporting Variantsnssv776017, nssv776011, nssv776010, nssv776019, nssv776014, nssv776016, nssv776018, nssv776015, nssv776013, nssv776012, nssv776008, nssv776009
Samples
Known GenesOR4C11, OR4C6, OR4P4, OR4S2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv554894
Frequency
Sample Size17421
Observed Gain1
Observed Loss11
Observed Complex0
Frequencyn/a


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