A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9756564



Internal ID18730810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:44733352..44733541hg38UCSC Ensembl
Outerchr21:44733346..44733569hg38UCSC Ensembl
Innerchr21:46153267..46153456hg19UCSC Ensembl
Outerchr21:46153261..46153484hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38224
hg19224
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3557817
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9756564
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