A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643525



Internal ID7030284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:5406687..5414694hg38UCSC Ensembl
Innerchr19:5406700..5414682hg38UCSC Ensembl
Outerchr19:5406675..5414707hg38UCSC Ensembl
chr19:5406698..5414705hg19UCSC Ensembl
Innerchr19:5406711..5414693hg19UCSC Ensembl
Outerchr19:5406686..5414718hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg388008
hg198008
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15982871
SamplesHG03673
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643525
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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