A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1290308



Internal ID12453431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:12090136..12090234hg38UCSC Ensembl
chr1:12150193..12150291hg19UCSC Ensembl
chr1:12072780..12072878hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3899
hg1999
hg1899
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4317882
SamplesHuRef
Known GenesTNFRSF8
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1290308
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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