A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2666431



Internal ID9585850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:16889571..16889742hg38UCSC Ensembl
Outerchr19:16889534..16889792hg38UCSC Ensembl
Innerchr19:17000382..17000553hg19UCSC Ensembl
Outerchr19:17000345..17000603hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38259
hg19259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5870025
SamplesNA12155
Known GenesF2RL3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2666431
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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