A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643780



Internal ID7030538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15874251..15906601hg38UCSC Ensembl
Innerchr19:15874301..15906551hg38UCSC Ensembl
Outerchr19:15874201..15906651hg38UCSC Ensembl
chr19:15985061..16017411hg19UCSC Ensembl
Innerchr19:15985111..16017361hg19UCSC Ensembl
Outerchr19:15985011..16017461hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3832351
hg1932351
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16002624, essv16002625, essv16002623
SamplesNA19054, NA19010, NA19011
Known GenesCYP4F2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643780
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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