A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453070



Internal ID21110623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:96852101..96856700hg38UCSC Ensembl
chr9:99614383..99618982hg19UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg384600
hg194600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223588
Samples
Known GenesZNF782
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453070
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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