A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642760



Internal ID7029529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:62945219..62996043hg38UCSC Ensembl
chr18:60612452..60663276hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3850825
hg1950825
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv620e214
Supporting Variantsessv15903424, essv15903425, essv15903428, essv15903426, essv15903427
SamplesHG03907, HG00368, HG00373, HG04017, HG00366
Known GenesPHLPP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642760
Frequency
Sample Size2504
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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