A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644372



Internal ID6684440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41119456..41147784hg38UCSC Ensembl
chr19:41625361..41653689hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3828329
hg1928329
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16055672
SamplesHG04134
Known GenesCYP2F1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644372
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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