A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1759060



Internal ID12922178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100511551..100511614hg38UCSC Ensembl
chr15:101051756..101051819hg19UCSC Ensembl
chr15:98869279..98869342hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3864
hg1964
hg1864
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4227686
SamplesHuRef
Known GenesCERS3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1759060
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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