A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444087



Internal ID21101640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:97945601..98224000hg38UCSC Ensembl
chr9:100707883..100986282hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg38278400
hg19278400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235398
Samples
Known GenesANP32B, CORO2A, NANS, TBC1D2, TRIM14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444087
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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