A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3201732



Internal ID22350992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27160793..27161419hg38UCSC Ensembl
chr1:27487284..27487910hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38627
hg19627
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14357557
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3201732
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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