A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677701



Internal ID9943806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:2969568..2970959hg38UCSC Ensembl
chr19:2969566..2970957hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381392
hg191392
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5689526
SamplesNA18951
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677701
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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