A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3527619



Internal ID22397006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:109356640..109361833hg38UCSC Ensembl
chr9:112118920..112124113hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg385194
hg195194
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14348306, nssv14348305
SamplesHG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3527619
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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