A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5749798



Internal ID9520355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:132040001..132045704hg38UCSC Ensembl
chr9:134915388..134921091hg19UCSC Ensembl
Cytoband9q34.13
Allele length
AssemblyAllele length
hg385704
hg195704
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662096
Supporting Variants
SamplesNA19007
Known GenesMED27
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5749798
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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