A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3771350



Internal ID18967622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:17801096..17801451hg38UCSC Ensembl
chr22:18283862..18284217hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38356
hg19356
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072614
Supporting Variants
SamplesKWP1
Known GenesMICAL3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3771350
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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