A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3219599



Internal ID22364575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28774801..28775129hg38UCSC Ensembl
chr17:27101819..27102147hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14391370
SamplesHG00733
Known GenesFAM222B
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3219599
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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