A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5569786



Internal ID9717099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:56353647..56358453hg38UCSC Ensembl
Outerchr19:56353276..56358823hg38UCSC Ensembl
Innerchr19:56865016..56869822hg19UCSC Ensembl
Outerchr19:56864645..56870192hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg385548
hg195548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2678539
Supporting Variants
SamplesNA19469
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5569786
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