A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046903



Internal ID19136122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:96481372..96546628hg38UCSC Ensembl
Innerchr11:96214536..96279793hg19UCSC Ensembl
Innerchr11:95854184..95919441hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3865257
hg1965258
hg1865258
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1256n100
Supporting Variantsnssv3509362
Samples
Known GenesJRKL-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046903
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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