A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3195169



Internal ID22345387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24543444..24543941hg38UCSC Ensembl
chr1:24869935..24870432hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg38498
hg19498
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14356500, nssv14356501
SamplesHG00512, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3195169
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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