A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418534



Internal ID21076087
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 StatusM
Merged Variants
Supporting Variantsnssv18217332
Samples
Known GenesKLHL9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418534
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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