A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525362



Internal ID22394740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99263587..99263652hg38UCSC Ensembl
chr3:98982431..98982496hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6086n152
Supporting Variantsnssv14308985, nssv14308987, nssv14308989, nssv14308988, nssv14308986
SamplesHG00512, HG00732, HG00733, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525362
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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