A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6038060



Internal ID9457288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:55397419..55399206hg38UCSC Ensembl
chr19:55908787..55910574hg19UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg381788
hg191788
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2662012
Supporting Variants
SamplesNA18908
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6038060
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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