A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2667969



Internal ID9587388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:10311332..10312441hg38UCSC Ensembl
Outerchr19:10311295..10312491hg38UCSC Ensembl
Innerchr19:10422008..10423117hg19UCSC Ensembl
Outerchr19:10421971..10423167hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381197
hg191197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6105750
SamplesNA19661
Known GenesFDX1L
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2667969
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer