A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672523



Internal ID9591942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89360850..89362792hg38UCSC Ensembl
chr14:89827194..89829136hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg381943
hg191943
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5655138, essv6244430, essv5594698, essv6513360, essv6013770
SamplesNA19055, HG01133, HG01550, NA20765, HG01137
Known GenesFOXN3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672523
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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