A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766396



Internal ID19306304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:20346708..20362310hg38UCSC Ensembl
chr22:20700999..20716600hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3815603
hg1915602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078508
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766396
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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