A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226304



Internal ID22369150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:8574537..8574595hg38UCSC Ensembl
chr19:8639421..8639479hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4125n152
Supporting Variantsnssv14285912, nssv14285913
SamplesHG00731, HG00733
Known GenesMYO1F
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226304
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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