A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3211176



Internal ID22358823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135534367..135534428hg38UCSC Ensembl
chr9:138426213..138426274hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9817n152
Supporting Variantsnssv14348745, nssv14348746, nssv14348744
SamplesNA19238, NA19239, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3211176
Frequency
Sample Size9
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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