A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955166



Internal ID16957353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:43238095..43320894hg38UCSC Ensembl
Outerchr22:43634101..43716900hg19UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3882800
hg1982800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000812
SamplesBILGI_BIOE
Known GenesSCUBE1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955166
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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