A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442132



Internal ID21099685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77021201..77025400hg38UCSC Ensembl
chr9:79636117..79640316hg19UCSC Ensembl
Cytoband9q21.2
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231026
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442132
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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