A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051109



Internal ID19140328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134469799..134860013hg38UCSC Ensembl
Innerchr11:134339693..134729907hg19UCSC Ensembl
Innerchr11:133844903..134235117hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38390215
hg19390215
hg18390215
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1308n100
Supporting Variantsnssv3513564
Samples
Known GenesLOC283177
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051109
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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