A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044260



Internal ID18786791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:131036593..131369909hg38UCSC Ensembl
Innerchr11:130906488..131239804hg19UCSC Ensembl
Innerchr11:130411698..130745014hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38333317
hg19333317
hg18333317
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1297n100
Supporting Variantsnssv3514034
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)nsv1044260
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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