A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1139065



Internal ID19262674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:39043404..39043471hg38UCSC Ensembl
Outerchr22:39439409..39439476hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3991691
SamplesKWS2
Known GenesAPOBEC3F
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1139065
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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