A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039379



Internal ID18781910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:59032901..59097071hg38UCSC Ensembl
Innerchr11:58800374..58864544hg19UCSC Ensembl
Innerchr11:58556950..58621120hg18UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3864171
hg1964171
hg1864171
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1208n100
Supporting Variantsnssv3511034, nssv3511624, nssv3509119
Samples
Known GenesLOC283194
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039379
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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