A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3560804



Internal ID22429601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:63488529..63488529hg38UCSC Ensembl
chr17:61565890..61565890hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14376252, nssv14384655
SamplesNA19238, NA19240
Known GenesACE
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3560804
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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