A curated catalogue of human genomic structural variation




Variant Details

Variant: essv4363772



Internal ID11299624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89360758..89360758hg38UCSC Ensembl
chr14:89827102..89827102hg19UCSC Ensembl
chr14:88896855..88896855hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38198
hg19198
hg18198
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1286606
Supporting Variants
SamplesHuRef
Known GenesFOXN3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv4363772
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer