A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3191053



Internal ID22341817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28250928..28251506hg38UCSC Ensembl
chr1:28577439..28578017hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg38579
hg19579
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14358240, nssv14358241
SamplesHG00512, NA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3191053
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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