A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5995572



Internal ID9906406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40854807..40886591hg38UCSC Ensembl
chr19:41360712..41392496hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3831785
hg1931785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv2676662
Supporting Variants
SamplesNA20801
Known GenesCYP2A7
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5995572
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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