A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046306



Internal ID18788837
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:68933054..68969593hg38UCSC Ensembl
Innerchr11:68700522..68737062hg19UCSC Ensembl
Innerchr11:68457098..68493638hg18UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3836540
hg1936541
hg1836541
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710639
Samples
Known GenesIGHMBP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046306
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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