A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6167210



Internal ID8907034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40117179..40119395hg38UCSC Ensembl
chr19:40623086..40625302hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg382217
hg192217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2660553
Supporting Variants
SamplesHG00369
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6167210
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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