A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044174



Internal ID19133393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55734320..56094696hg38UCSC Ensembl
Innerchr11:55501796..55862172hg19UCSC Ensembl
Innerchr11:55258372..55618748hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg38360377
hg19360377
hg18360377
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710603
Samples
Known GenesOR10AG1, OR5AS1, OR5D13, OR5D14, OR5D16, OR5D18, OR5F1, OR5I1, OR5L1, OR5L2, OR5W2, OR7E5P, OR8I2, TRIM51
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044174
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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