A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643839



Internal ID7030596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:18469638..18490124hg38UCSC Ensembl
chr19:18580448..18600934hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3820487
hg1920487
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16003962, essv16003961
SamplesHG03380, HG03446
Known GenesELL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643839
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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