A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525190



Internal ID22394566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154389833..154390203hg38UCSC Ensembl
chr1:154362309..154362679hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38371
hg19371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14287121, nssv14287122, nssv14287120
SamplesHG00731, HG00732, HG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525190
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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