A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643511



Internal ID7030270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4798988..4800227hg38UCSC Ensembl
Innerchr19:4798989..4800227hg38UCSC Ensembl
Outerchr19:4798988..4800228hg38UCSC Ensembl
chr19:4799000..4800239hg19UCSC Ensembl
Innerchr19:4799001..4800239hg19UCSC Ensembl
Outerchr19:4799000..4800240hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381240
hg191240
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15982234
SamplesNA18545
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643511
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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