A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641774



Internal ID7028545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10327446..10347699hg38UCSC Ensembl
chr18:10327443..10347696hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3820254
hg1920254
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv600e214
Supporting Variantsessv15804484
SamplesNA21097
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641774
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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