A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5806902



Internal ID9739790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178681255..178688092hg38UCSC Ensembl
chr5:178108256..178115093hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg386838
hg196838
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657021
Supporting Variants
SamplesNA19675
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5806902
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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