A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5579914



Internal ID8557317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:19666564..19674436hg38UCSC Ensembl
chr19:19777373..19785245hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg387873
hg197873
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659968
Supporting Variants
SamplesHG01171
Known GenesZNF101
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5579914
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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