A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16055672



Internal ID6057488
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644372
Supporting Variants
SamplesHG04134
Known GenesCYP2F1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16055672
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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