A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5415827



Internal ID8393230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14199550..14200453hg38UCSC Ensembl
chr10:14241549..14242452hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38904
hg19904
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2657983
Supporting Variants
SamplesHG00112
Known GenesFRMD4A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5415827
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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