A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643359



Internal ID6683439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:656766..668988hg38UCSC Ensembl
chr19:656766..668988hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3812223
hg1912223
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15967924
SamplesHG00867
Known GenesRNF126
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643359
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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