A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038296



Internal ID19127515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:96757982..96796409hg38UCSC Ensembl
Innerchr11:96628982..96667409hg19UCSC Ensembl
Innerchr11:96134192..96172619hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3838428
hg1938428
hg1838428
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3508414
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)nsv1038296
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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