A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220586



Internal ID20787626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:525192..815611hg38UCSC Ensembl
chr9:525192..815611hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38290420
hg19290420
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6432288
Supporting Variants
Samples
Known GenesKANK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220586
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00018


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