A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643771



Internal ID7030529
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:15567761..15586004hg38UCSC Ensembl
Innerchr19:15567761..15586004hg38UCSC Ensembl
Outerchr19:15567261..15586504hg38UCSC Ensembl
chr19:15678572..15696815hg19UCSC Ensembl
Innerchr19:15678572..15696815hg19UCSC Ensembl
Outerchr19:15678072..15697315hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3818244
hg1918244
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15999980, essv15999981
SamplesNA18877, NA19235
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643771
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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