A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644899



Internal ID7031650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57225938..57227501hg38UCSC Ensembl
Innerchr19:57225938..57227501hg38UCSC Ensembl
Outerchr19:57225717..57227747hg38UCSC Ensembl
chr19:57737306..57738869hg19UCSC Ensembl
Innerchr19:57737306..57738869hg19UCSC Ensembl
Outerchr19:57737085..57739115hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg381564
hg191564
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16107174, essv16107173
SamplesHG00731, HG01395
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644899
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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