A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5668337



Internal ID9351455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:135966628..135999292hg38UCSC Ensembl
Outerchr5:135966591..135999342hg38UCSC Ensembl
Innerchr5:135302317..135334981hg19UCSC Ensembl
Outerchr5:135302280..135335031hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3832752
hg1932752
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659848
Supporting Variants
SamplesNA18547
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5668337
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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