A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3227185



Internal ID22369758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37911366..38263088hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg38351723
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14373574, nssv14388390
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3227185
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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