A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3647704



Internal ID7034444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37164411..37165067hg38UCSC Ensembl
Innerchr22:37164461..37164925hg38UCSC Ensembl
Outerchr22:37164361..37165117hg38UCSC Ensembl
chr22:37560451..37561107hg19UCSC Ensembl
Innerchr22:37560501..37560965hg19UCSC Ensembl
Outerchr22:37560401..37561157hg19UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg38657
hg19657
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16420831, essv16420829, essv16420830, essv16420828
SamplesHG03237, NA20814, HG01699, HG01697
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3647704
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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