A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5830980



Internal ID9597862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:15906418..15912553hg38UCSC Ensembl
chr5:15906527..15912662hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg386136
hg196136
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2672541
Supporting Variants
SamplesNA19235
Known GenesFBXL7
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5830980
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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