A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226306



Internal ID22369151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63993240..63994918hg38UCSC Ensembl
chr17:62070600..62072278hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg381679
hg191679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14392067
SamplesHG00512
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226306
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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