A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220068



Internal ID20787108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69065301..69189629hg38UCSC Ensembl
chr9:71680217..71804545hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg38124329
hg19124329
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446318
Supporting Variants
Samples
Known GenesFXN, TJP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220068
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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