A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553768



Internal ID16341177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:23761792..23819629hg38UCSC Ensembl
Innerchr11:23783338..23841175hg19UCSC Ensembl
Innerchr11:23739914..23797751hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3857838
hg1957838
hg1857838
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1696n54
Supporting Variantsnssv1174752, nssv768968, nssv1174751, nssv768965, nssv768967, nssv768966
Samples1780862310_A, 1780854341_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553768
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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