A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3193075



Internal ID22343567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:28569098..28576294hg38UCSC Ensembl
chr3:28610589..28617785hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg387197
hg197197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14307201
SamplesHG00731
Known GenesLINC00693
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3193075
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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