A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3561689



Internal ID22430457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27652840..27652840hg38UCSC Ensembl
chr1:27979351..27979351hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3883
hg1983
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14357664, nssv14357665
SamplesHG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3561689
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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