A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042423



Internal ID19131642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:92454139..92489405hg38UCSC Ensembl
Innerchr11:92187305..92222571hg19UCSC Ensembl
Innerchr11:91826953..91862219hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3835267
hg1935267
hg1835267
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710707
Samples
Known GenesFAT3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042423
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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