A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6460406



Internal ID9905896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9518673..9525739hg38UCSC Ensembl
chr19:9629349..9636415hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg387067
hg197067
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2665615
Supporting Variants
SamplesNA20801
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6460406
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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