A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3563677



Internal ID22432413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:119993635..119993635hg38UCSC Ensembl
chr4:120914790..120914790hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14316420, nssv14316421
SamplesHG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3563677
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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