A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3562753



Internal ID22431499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177432890..177432890hg38UCSC Ensembl
chr3:177150678..177150678hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3861
hg1961
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14311610, nssv14311611
SamplesHG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3562753
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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