A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1686273



Internal ID12849391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24881555..24881613hg38UCSC Ensembl
chr15:25126702..25126760hg19UCSC Ensembl
chr15:22677795..22677853hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3859
hg1959
hg1859
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3735303
SamplesHuRef
Known GenesSNRPN
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1686273
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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