A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043139



Internal ID19132358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107854571..107998490hg38UCSC Ensembl
Innerchr11:107725297..107869216hg19UCSC Ensembl
Innerchr11:107230507..107374426hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38143920
hg19143920
hg18143920
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3514837
Samples
Known GenesRAB39A, SLC35F2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043139
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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