A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437713



Internal ID21095266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:91139004..91147445hg38UCSC Ensembl
chr9:93901286..93909727hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg388442
hg198442
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223811
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437713
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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