A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955186



Internal ID16957373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:48484289..48570188hg38UCSC Ensembl
Outerchr22:48880101..48966000hg19UCSC Ensembl
Cytoband22q13.32
Allele length
AssemblyAllele length
hg3885900
hg1985900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000832
SamplesBILGI_BIOE
Known GenesFAM19A5, LOC284933
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955186
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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