A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039671



Internal ID19128890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:68353103..68439162hg38UCSC Ensembl
Innerchr11:68120571..68206630hg19UCSC Ensembl
Innerchr11:67877147..67963206hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3886060
hg1986060
hg1886060
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3509412
Samples
Known GenesLRP5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039671
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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