A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9853416



Internal ID3209798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:11000055..11002253hg38UCSC Ensembl
Innerchr1:11000055..11002253hg38UCSC Ensembl
Outerchr1:11000055..11002253hg38UCSC Ensembl
chr1:11060112..11062310hg19UCSC Ensembl
Innerchr1:11060112..11062310hg19UCSC Ensembl
Outerchr1:11060112..11062310hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg382199
hg192199
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3585211
Supporting Variants
SamplesHG02814
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv9853416
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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