A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5401858



Internal ID9171203
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35627672..35628077hg38UCSC Ensembl
chr19:36118574..36118979hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38406
hg19406
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2657778
Supporting Variants
SamplesHG01375
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5401858
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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