A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3644876



Internal ID7031627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56739576..56768809hg38UCSC Ensembl
Innerchr19:56739576..56768809hg38UCSC Ensembl
Outerchr19:56739076..56769309hg38UCSC Ensembl
chr19:57250944..57280177hg19UCSC Ensembl
Innerchr19:57250944..57280177hg19UCSC Ensembl
Outerchr19:57250444..57280677hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3829234
hg1929234
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16103389
SamplesNA18611
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3644876
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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