A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv784148



Internal ID16078104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107368911..107372195hg38UCSC Ensembl
Innerchr11:107239637..107242921hg19UCSC Ensembl
Innerchr11:106744847..106748131hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg383285
hg193285
hg183285
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556331
Supporting Variants
Samples
Known GenesCWF19L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv784148
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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