A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2664700



Internal ID9584119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:4864379..4871476hg38UCSC Ensembl
Outerchr19:4864342..4871526hg38UCSC Ensembl
Innerchr19:4864391..4871488hg19UCSC Ensembl
Outerchr19:4864354..4871538hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg387185
hg197185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5564077
SamplesNA20588
Known GenesPLIN3
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2664700
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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