A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2668617



Internal ID9588036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94613949..94614408hg38UCSC Ensembl
chr9:97376231..97376690hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg38460
hg19460
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6084566, essv6286199, essv6579139, essv5872233, essv6121266, essv5943030
SamplesHG00173, HG00326, HG00244, HG00242, HG00231, HG01066
Known GenesFBP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2668617
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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