A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5808657



Internal ID8786060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137780167..137780318hg38UCSC Ensembl
chr9:140674619..140674770hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2676307
Supporting Variants
SamplesNA19311
Known GenesEHMT1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5808657
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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