A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442759



Internal ID21100312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81859867..81903153hg38UCSC Ensembl
chr9:84474782..84518068hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3843287
hg1943287
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227389
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442759
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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