A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043591



Internal ID19132810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:113610250..113652259hg38UCSC Ensembl
Innerchr11:113480972..113522981hg19UCSC Ensembl
Innerchr11:112986182..113028191hg18UCSC Ensembl
Cytoband11q23.2
Allele length
AssemblyAllele length
hg3842010
hg1942010
hg1842010
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710751, nssv3710750
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043591
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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