A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1144764



Internal ID12307887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133111855..133111855hg38UCSC Ensembl
chr10:134925359..134925359hg19UCSC Ensembl
chr10:134775349..134775349hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38252
hg19252
hg18252
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3741657
SamplesHuRef
Known GenesGPR123
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1144764
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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