A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667087



Internal ID9586506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1612633..1613105hg38UCSC Ensembl
chr19:1612632..1613104hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38473
hg19473
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5774573, essv6109479, essv5402349, essv6122030
SamplesHG00272, HG01488, HG00183, HG01055
Known GenesTCF3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667087
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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