A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672541



Internal ID9938646
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 StatusM
Merged Variants
Supporting Variantsessv5780564, essv5772399, essv5644310, essv5778204, essv5829124, essv6494040, essv5478551, essv5830980, essv5423006, essv5844489, essv6019238
SamplesNA19466, NA19916, NA19917, NA19235, NA19471, NA18516, NA19453, NA19375, HG01342, NA19398, NA19430
Known GenesFBXL7
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672541
Frequency
Sample Size1151
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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