A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670459



Internal ID9589878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:32717968..32732968hg38UCSC Ensembl
Outerchr19:32717931..32733018hg38UCSC Ensembl
Innerchr19:33208874..33223874hg19UCSC Ensembl
Outerchr19:33208837..33223924hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3815088
hg1915088
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6007770
SamplesNA11892
Known GenesTDRD12
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670459
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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