A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18217332



Internal ID20784372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:21330601..21337600hg38UCSC Ensembl
chr9:21330600..21337599hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg387000
hg197000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6418534
Supporting Variants
Samples
Known GenesKLHL9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18217332
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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