A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643428



Internal ID7030190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2502951..2507905hg38UCSC Ensembl
Innerchr19:2502951..2507905hg38UCSC Ensembl
Outerchr19:2502683..2508152hg38UCSC Ensembl
chr19:2502949..2507903hg19UCSC Ensembl
Innerchr19:2502949..2507903hg19UCSC Ensembl
Outerchr19:2502681..2508150hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg384955
hg194955
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15969567
SamplesNA18595
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643428
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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