A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5476464



Internal ID9835926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:106582761..106583142hg38UCSC Ensembl
chr1:107125383..107125764hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38382
hg19382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2658150
Supporting Variants
SamplesNA20346
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5476464
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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