A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3198088



Internal ID22347865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:90812589..90813080hg38UCSC Ensembl
chr1:91278146..91278637hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg38492
hg19492
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14382832
SamplesHG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3198088
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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