A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6562063



Internal ID9509941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:10217232..10223763hg38UCSC Ensembl
Outerchr18:10217195..10223813hg38UCSC Ensembl
Innerchr18:10217229..10223760hg19UCSC Ensembl
Outerchr18:10217192..10223810hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg386619
hg196619
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2662157
Supporting Variants
SamplesNA18989
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6562063
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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