A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953069



Internal ID16955256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:31081515..31107614hg38UCSC Ensembl
Outerchr22:31477501..31503600hg19UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg3826100
hg1926100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000791
SamplesBILGI_BIOE
Known GenesSELM, SMTN
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953069
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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