A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1144980



Internal ID19263535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:49826852..49827952hg38UCSC Ensembl
Outerchr22:50220500..50221600hg19UCSC Ensembl
Cytoband22q13.33
Allele length
AssemblyAllele length
hg381101
hg191101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3981590
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1144980
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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