A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5907021



Internal ID8884424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:10689450..10689690hg38UCSC Ensembl
Outerchr18:10689413..10689740hg38UCSC Ensembl
Innerchr18:10689448..10689688hg19UCSC Ensembl
Outerchr18:10689411..10689738hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2675075
Supporting Variants
SamplesNA19776
Known GenesPIEZO2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5907021
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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