A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669455



Internal ID9935560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3530286..3530500hg38UCSC Ensembl
chr19:3530284..3530498hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38215
hg19215
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6511174, essv5541091, essv5460516, essv6130316, essv6074886, essv6411101
SamplesNA19359, NA19197, NA19371, NA19391, HG00500, NA19114
Known GenesFZR1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669455
Frequency
Sample Size1151
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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