A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3561290



Internal ID22430072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156004598..156004598hg38UCSC Ensembl
chr1:155974389..155974389hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14289392
SamplesHG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3561290
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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