A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035733



Internal ID18778264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:130509478..131429821hg38UCSC Ensembl
Innerchr11:130379373..131299715hg19UCSC Ensembl
Innerchr11:129884583..130804925hg18UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38920344
hg19920343
hg18920343
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3504086
Samples
Known GenesC11orf44, MIR8052, NTM, SNX19
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035733
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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