A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659519



Internal ID9925624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19690435..19691470hg38UCSC Ensembl
chr19:19801244..19802279hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg381036
hg191036
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6458794, essv5853212, essv5494081, essv5502131
SamplesNA19703, NA19374, NA19373, NA18501
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659519
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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