A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047031



Internal ID19136250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55921634..56060062hg38UCSC Ensembl
Innerchr11:55689110..55827538hg19UCSC Ensembl
Innerchr11:55445686..55584114hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38138429
hg19138429
hg18138429
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1206n100
Supporting Variantsnssv3516805
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)nsv1047031
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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