A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5807969



Internal ID9457247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:151964680..151970377hg38UCSC Ensembl
Outerchr1:151964523..151970530hg38UCSC Ensembl
Innerchr1:151937156..151942853hg19UCSC Ensembl
Outerchr1:151936999..151943006hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg386008
hg196008
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2656579
Supporting Variants
SamplesNA18908
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5807969
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