A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9756912



Internal ID18731158
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:38978115..38979486hg38UCSC Ensembl
Outerchr22:38978087..38979770hg38UCSC Ensembl
Innerchr22:39374120..39375491hg19UCSC Ensembl
Outerchr22:39374092..39375775hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg381684
hg191684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3558165
Supporting Variants
Samples
Known GenesAPOBEC3A_B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9756912
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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