A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5934509



Internal ID8795862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105652630..105751400hg38UCSC Ensembl
chr14:106118967..106217737hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3898771
hg1998771
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659213
Supporting Variants
SamplesHG00242
Known GenesELK2AP
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5934509
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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