A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6433523



Internal ID21091076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:41133..300048hg38UCSC Ensembl
chr9:41133..300048hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38258916
hg19258916
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236588
Samples
Known GenesC9orf66, CBWD1, DOCK8, FOXD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6433523
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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