A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662368



Internal ID9581787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9819438..9820577hg38UCSC Ensembl
Outerchr19:9819401..9820627hg38UCSC Ensembl
Innerchr19:9930114..9931253hg19UCSC Ensembl
Outerchr19:9930077..9931303hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381227
hg191227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6152985, essv6435969, essv5940896
SamplesHG00559, NA18560, HG00437
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662368
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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