A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556598



Internal ID15997321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134252356..134298912hg38UCSC Ensembl
Innerchr11:134122250..134168806hg19UCSC Ensembl
Innerchr11:133627460..133674016hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3846557
hg1946557
hg1846557
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv785143
Samples
Known GenesACAD8, GLB1L3, THYN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556598
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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