A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049333



Internal ID19138552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:98558658..98652026hg38UCSC Ensembl
Innerchr11:98429388..98522756hg19UCSC Ensembl
Innerchr11:97934598..98027966hg18UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg3893369
hg1993369
hg1893369
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3515869
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)nsv1049333
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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