A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6446990



Internal ID21104543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:80652701..80667100hg38UCSC Ensembl
chr9:83267616..83282015hg19UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg3814400
hg1914400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7846n223
Supporting Variantsnssv18234069
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6446990
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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