A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646445



Internal ID7033189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:15369640..15371337hg38UCSC Ensembl
Innerchr21:15369650..15371328hg38UCSC Ensembl
Outerchr21:15369631..15371347hg38UCSC Ensembl
chr21:16741959..16743656hg19UCSC Ensembl
Innerchr21:16741969..16743647hg19UCSC Ensembl
Outerchr21:16741950..16743666hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg381698
hg191698
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16268733
SamplesNA18960
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646445
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