A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3209189



Internal ID22357305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:194285687..194285739hg38UCSC Ensembl
chr3:194003476..194003528hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14310278
SamplesNA19238
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3209189
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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