A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4115967



Internal ID11398506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:60433802..60433802hg38UCSC Ensembl
chr14:60900520..60900520hg19UCSC Ensembl
chr14:59970273..59970273hg18UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3854
hg1954
hg1854
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1141736
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4115967
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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