A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642981



Internal ID7029750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:70021500..70048326hg38UCSC Ensembl
chr18:67688736..67715562hg19UCSC Ensembl
Cytoband18q22.2
Allele length
AssemblyAllele length
hg3826827
hg1926827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15930781
SamplesNA06984
Known GenesRTTN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642981
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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