A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv783738



Internal ID16077694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107368380..107369767hg38UCSC Ensembl
Innerchr11:107239106..107240493hg19UCSC Ensembl
Innerchr11:106744316..106745703hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381388
hg191388
hg181388
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556289
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)nssv783738
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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