A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050801



Internal ID19140020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55918323..56058703hg38UCSC Ensembl
Innerchr11:55685799..55826179hg19UCSC Ensembl
Innerchr11:55442375..55582755hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38140381
hg19140381
hg18140381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1206n100
Supporting Variantsnssv3513285, nssv3509036, nssv3511775, nssv3521652, nssv3513893, nssv3507466, nssv3505666, nssv3520351, nssv3517211, nssv3506103, nssv3510956, nssv3517601, nssv3505859, nssv3511662, nssv3504569, nssv3517575, nssv3515024, nssv3516811
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)nsv1050801
Frequency
Sample Size11257
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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