A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660627



Internal ID9926732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:16809034..16812629hg38UCSC Ensembl
Outerchr19:16809000..16812664hg38UCSC Ensembl
Innerchr19:16919845..16923440hg19UCSC Ensembl
Outerchr19:16919811..16923475hg19UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg383665
hg193665
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6081604
SamplesNA19734
Known GenesNWD1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660627
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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