A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6058858



Internal ID9252922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:101634255..101635335hg38UCSC Ensembl
chr10:103394012..103395092hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg381081
hg191081
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663159
Supporting Variants
SamplesNA12154
Known GenesFBXW4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6058858
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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