A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3770446



Internal ID19315002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:6841276..6841349hg38UCSC Ensembl
Outerchr20:6821923..6821996hg19UCSC Ensembl
Cytoband20p12.3
Allele length
AssemblyAllele length
hg3874
hg1974
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078928
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3770446
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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