A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659829



Internal ID9925934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:8270031..8272094hg38UCSC Ensembl
Outerchr19:8269997..8272129hg38UCSC Ensembl
Innerchr19:8334915..8336978hg19UCSC Ensembl
Outerchr19:8334881..8337013hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg382133
hg192133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv619e199
Supporting Variantsessv6179074
SamplesNA19471
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659829
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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