A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5616564



Internal ID9098741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:31102238..31104364hg38UCSC Ensembl
Outerchr1:31102081..31104517hg38UCSC Ensembl
Innerchr1:31575085..31577211hg19UCSC Ensembl
Outerchr1:31574928..31577364hg19UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg382437
hg192437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677324
Supporting Variants
SamplesHG01080
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5616564
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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