A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670076



Internal ID9936181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:40293474..40319812hg38UCSC Ensembl
Outerchr19:40293437..40319862hg38UCSC Ensembl
Innerchr19:40799381..40825719hg19UCSC Ensembl
Outerchr19:40799344..40825769hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3826426
hg1926426
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6302611
SamplesNA19082
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670076
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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