A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3769566



Internal ID18959495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38317094..38317395hg38UCSC Ensembl
chr22:38713099..38713400hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072637
Supporting Variants
SamplesKWP1
Known GenesCSNK1E
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3769566
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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