A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671080



Internal ID9937185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:11365995..11366636hg38UCSC Ensembl
Outerchr19:11365838..11366789hg38UCSC Ensembl
Innerchr19:11476671..11477312hg19UCSC Ensembl
Outerchr19:11476514..11477465hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38952
hg19952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5970490, essv5430631
SamplesNA19909, NA19398
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671080
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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