A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3220719



Internal ID22365333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:82510414..82510484hg38UCSC Ensembl
chr9:85125329..85125399hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv9624n152
Supporting Variantsnssv14347130, nssv14347129, nssv14347128, nssv14347131
SamplesHG00512, NA19238, NA19240, HG00513
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3220719
Frequency
Sample Size9
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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