A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5668916



Internal ID8646319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:45310891..45311354hg38UCSC Ensembl
chr19:45814149..45814612hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38464
hg19464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2660204
Supporting Variants
SamplesNA19371
Known GenesCKM
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5668916
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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