A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6293864



Internal ID9391467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:2502833..2507739hg38UCSC Ensembl
Outerchr19:2502796..2507789hg38UCSC Ensembl
Innerchr19:2502831..2507737hg19UCSC Ensembl
Outerchr19:2502794..2507787hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg384994
hg194994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676254
Supporting Variants
SamplesNA18595
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6293864
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