A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440573



Internal ID21098126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88315691..88328165hg38UCSC Ensembl
chr9:90930606..90943080hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg3812475
hg1912475
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219550
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440573
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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