A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670511



Internal ID9936616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:9134840..9135996hg38UCSC Ensembl
chr19:9245516..9246672hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381157
hg191157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6467707, essv6528526, essv6183932, essv5729591
SamplesHG00158, NA12044, NA12342, HG00372
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670511
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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