A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036874



Internal ID18779405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107777579..107809102hg38UCSC Ensembl
Innerchr11:107648305..107679828hg19UCSC Ensembl
Innerchr11:107153515..107185038hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg3831524
hg1931524
hg1831524
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3505553
Samples
Known GenesSLC35F2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036874
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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