A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3962140



Internal ID11799732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:5916689..5916689hg38UCSC Ensembl
chr10:5958652..5958652hg19UCSC Ensembl
chr10:5998658..5998658hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38164
hg19164
hg18164
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1168062
Supporting Variants
SamplesHuRef
Known GenesFBXO18
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3962140
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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