A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3563366



Internal ID22432103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:107911811..107911811hg38UCSC Ensembl
chr4:108832967..108832967hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14316927
SamplesHG00732
Known GenesSGMS2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3563366
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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