A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955185



Internal ID16957372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:47619352..47633051hg38UCSC Ensembl
Outerchr22:48015101..48028800hg19UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3813700
hg1913700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000831
SamplesBILGI_BIOE
Known GenesLINC00898
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955185
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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