A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3995008



Internal ID11420179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89362686..89362746hg38UCSC Ensembl
chr14:89829030..89829090hg19UCSC Ensembl
chr14:88898783..88898843hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3861
hg1961
hg1861
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1491660
Supporting Variants
SamplesHuRef
Known GenesFOXN3
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)essv3995008
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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