A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053414



Internal ID19142633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:5591759..6008982hg38UCSC Ensembl
Innerchr11:5612989..6030212hg19UCSC Ensembl
Innerchr11:5569565..5986788hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38417224
hg19417224
hg18417224
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3522446
Samples
Known GenesOR52E4, OR52E6, OR52E8, OR52L1, OR52N1, OR52N2, OR52N4, OR52N5, OR56A3, OR56A4, OR56A5, OR56B1, TRIM22, TRIM34, TRIM5, TRIM6, TRIM6-TRIM34
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053414
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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