A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6016408



Internal ID9533039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:41569172..41582606hg38UCSC Ensembl
chr5:41569274..41582708hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg3813435
hg1913435
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663060
Supporting Variants
SamplesNA19063
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6016408
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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