A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3528381



Internal ID22397768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:120494746..120497452hg38UCSC Ensembl
chr9:123257024..123259730hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg382707
hg192707
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9735n152
Supporting Variantsnssv14349836, nssv14349835
SamplesNA19239, NA19240
Known GenesCDK5RAP2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3528381
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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