A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3563287



Internal ID22432025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42912637..42912637hg38UCSC Ensembl
chr3:42954129..42954129hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14306775
SamplesNA19238
Known GenesZNF662
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3563287
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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