A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043388



Internal ID19132607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:102146988..102302126hg38UCSC Ensembl
Innerchr11:102017719..102172857hg19UCSC Ensembl
Innerchr11:101522929..101678067hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38155139
hg19155139
hg18155139
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3509898
Samples
Known GenesYAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043388
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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