A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5539556



Internal ID9095984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77885698..77886925hg38UCSC Ensembl
chr5:77181522..77182749hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg381228
hg191228
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2660618
Supporting Variants
SamplesHG01079
Known GenesLOC101929154
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5539556
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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