A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5907129



Internal ID9455912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:134181997..134183658hg38UCSC Ensembl
chr8:135194240..135195901hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg381662
hg191662
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2673733
Supporting Variants
SamplesNA18907
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5907129
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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