A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669191



Internal ID9935296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:4835478..4836358hg38UCSC Ensembl
chr19:4835490..4836370hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38881
hg19881
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5653417, essv6437976, essv6489375, essv5751096, essv6465458, essv5804881, essv5693880, essv5900811, essv6110679
SamplesNA18592, NA18988, NA18619, HG00613, NA19003, HG00476, NA18943, NA18624, NA18623
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669191
Frequency
Sample Size1151
Observed Gain0
Observed Loss9
Observed Complex0
Frequencyn/a


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