A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9756904



Internal ID18731150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38217264..38217416hg38UCSC Ensembl
Outerchr22:38217260..38217418hg38UCSC Ensembl
Innerchr22:38613271..38613423hg19UCSC Ensembl
Outerchr22:38613267..38613425hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558157
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9756904
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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