A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556349



Internal ID16343758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:107369523..107372701hg38UCSC Ensembl
Innerchr11:107240249..107243427hg19UCSC Ensembl
Innerchr11:106745459..106748637hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg383179
hg193179
hg183179
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2169n54
Supporting Variantsnssv784173, nssv784172
Samples
Known GenesCWF19L2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556349
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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