A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641562



Internal ID6681647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:2395070..2566412hg38UCSC Ensembl
chr18:2395069..2566411hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38171343
hg19171343
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15778132, essv15778133, essv15778131
SamplesNA19466, NA20858, NA19035
Known GenesMETTL4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641562
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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