A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5833014



Internal ID8810417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:22345419..22348055hg38UCSC Ensembl
chr8:22202932..22205568hg19UCSC Ensembl
Cytoband8p21.3
Allele length
AssemblyAllele length
hg382637
hg192637
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2669515
Supporting Variants
SamplesHG00254
Known GenesPIWIL2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5833014
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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