A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039087



Internal ID18781618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:131230668..131438530hg38UCSC Ensembl
Innerchr11:131100563..131308424hg19UCSC Ensembl
Innerchr11:130605773..130813634hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38207863
hg19207862
hg18207862
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3507037
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)nsv1039087
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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