A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556643



Internal ID16344052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134484618..134849175hg38UCSC Ensembl
Innerchr11:134354512..134719069hg19UCSC Ensembl
Innerchr11:133859722..134224279hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38364558
hg19364558
hg18364558
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2207n54
Supporting Variantsnssv1176226, nssv785185
Samples1780862484_A
Known GenesLOC283177
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556643
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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