A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525291



Internal ID22394667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195023324..195023582hg38UCSC Ensembl
chr3:194744053..194744311hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38259
hg19259
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14310336, nssv14310335
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525291
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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