A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16041240



Internal ID3660582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:32538051..32550238hg38UCSC Ensembl
Innerchr19:32538062..32550227hg38UCSC Ensembl
Outerchr19:32538040..32550249hg38UCSC Ensembl
chr19:33028957..33041144hg19UCSC Ensembl
Innerchr19:33028968..33041133hg19UCSC Ensembl
Outerchr19:33028946..33041155hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3812188
hg1912188
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3644172
Supporting Variants
SamplesHG03259
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv16041240
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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