A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1462632



Internal ID12279068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:106725154..106725451hg38UCSC Ensembl
chr11:106595880..106596177hg19UCSC Ensembl
chr11:106101090..106101387hg18UCSC Ensembl
Cytoband11q22.3
Allele length
AssemblyAllele length
hg38298
hg19298
hg18298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4159941
SamplesHuRef
Known GenesGUCY1A2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1462632
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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