A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438739



Internal ID21096292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:83773699..83837031hg38UCSC Ensembl
chr9:86388614..86451946hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3863333
hg1963333
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232942
Samples
Known GenesGKAP1, KIF27
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438739
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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