A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556636



Internal ID16344045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134479860..134851577hg38UCSC Ensembl
Innerchr11:134349754..134721471hg19UCSC Ensembl
Innerchr11:133854964..134226681hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38371718
hg19371718
hg18371718
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2207n54
Supporting Variantsnssv1176222
Samples1780862540_A
Known GenesLOC283177
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556636
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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