A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643486



Internal ID7030247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4007999..4017675hg38UCSC Ensembl
chr19:4007997..4017673hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg389677
hg199677
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15980293, essv15980291, essv15980292
SamplesNA18999, NA19067, NA18978
Known GenesPIAS4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643486
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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