A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643850



Internal ID6683919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19325949..19330159hg38UCSC Ensembl
Innerchr19:19326449..19329659hg38UCSC Ensembl
Outerchr19:19324949..19331159hg38UCSC Ensembl
chr19:19436758..19440968hg19UCSC Ensembl
Innerchr19:19437258..19440468hg19UCSC Ensembl
Outerchr19:19435758..19441968hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg384211
hg194211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16005706, essv16005707
SamplesHG02009, HG02594
Known GenesMAU2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643850
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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