A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053592



Internal ID19142811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55918323..56052471hg38UCSC Ensembl
Innerchr11:55685799..55819947hg19UCSC Ensembl
Innerchr11:55442375..55576523hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38134149
hg19134149
hg18134149
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1206n100
Supporting Variantsnssv3520046
Samples
Known GenesOR10AG1, OR5AS1, OR5F1, OR5I1, OR7E5P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053592
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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