A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641783



Internal ID6681865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10910699..10923469hg38UCSC Ensembl
Innerchr18:10910699..10923469hg38UCSC Ensembl
Outerchr18:10910199..10923969hg38UCSC Ensembl
chr18:10910697..10923467hg19UCSC Ensembl
Innerchr18:10910697..10923467hg19UCSC Ensembl
Outerchr18:10910197..10923967hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg3812771
hg1912771
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15804537
SamplesHG00268
Known GenesPIEZO2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641783
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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