A curated catalogue of human genomic structural variation




Variant Details

Variant: esv997476



Internal ID6733418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:106725144..106725440hg38UCSC Ensembl
chr11:106595870..106596166hg19UCSC Ensembl
chr11:106101080..106101376hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38297
hg19297
hg18297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3573693
SamplesHuRef
Known GenesGUCY1A2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)esv997476
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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