A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555670



Internal ID16343079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:86571638..86575599hg38UCSC Ensembl
Innerchr11:86282680..86286641hg19UCSC Ensembl
Innerchr11:85960328..85964289hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg383962
hg193962
hg183962
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2046n54
Supporting Variantsnssv779980, nssv779987, nssv779976, nssv779970, nssv779973, nssv779984, nssv779981, nssv779971, nssv779979, nssv779982, nssv779967, nssv779977, nssv779975, nssv779974, nssv779988, nssv779972, nssv779985, nssv779969, nssv779978, nssv779986, nssv779968, nssv779983
Samples
Known GenesME3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555670
Frequency
Sample Size17421
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


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