A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2157n54



Internal ID20135581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:106915702..106917261hg38UCSC Ensembl
chr11:106786428..106787987hg19UCSC Ensembl
chr11:106291638..106293197hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg381560
hg191560
hg181560
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv556239, nsv556256, nsv556249, nsv556240, nsv556248, nsv556238
Samples
Known GenesGUCY1A2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv2157n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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