A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048620



Internal ID18791151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:80377395..81970531hg38UCSC Ensembl
Innerchr11:80088439..81681573hg19UCSC Ensembl
Innerchr11:79766087..81359221hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg381593137
hg191593135
hg181593135
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3518299
Samples
Known GenesMIR4300
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048620
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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