A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3561820



Internal ID22430588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37102938..37102938hg38UCSC Ensembl
chr1:37568539..37568539hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14362311, nssv14362313, nssv14362312
SamplesHG00731, HG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3561820
Frequency
Sample Size9
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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