A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3965711



Internal ID18895977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:17801130..17801452hg38UCSC Ensembl
Outerchr22:18283896..18284218hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38323
hg19323
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1130447
Supporting Variants
SamplesKWS2
Known GenesMICAL3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3965711
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