A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3893600



Internal ID11521585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89361384..89362210hg38UCSC Ensembl
chr14:89827728..89828554hg19UCSC Ensembl
chr14:88897481..88898307hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38827
hg19827
hg18827
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1552920
Supporting Variants
SamplesHuRef
Known GenesFOXN3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3893600
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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