A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038589



Internal ID18781120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:131485121..131529812hg38UCSC Ensembl
Innerchr11:131355015..131399706hg19UCSC Ensembl
Innerchr11:130860225..130904916hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3844692
hg1944692
hg1844692
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1298n100
Supporting Variantsnssv3510244
Samples
Known GenesNTM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038589
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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