A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231684



Internal ID20798724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:72598..452686hg38UCSC Ensembl
chr9:72598..452686hg19UCSC Ensembl
Cytoband9p24.3
Allele length
AssemblyAllele length
hg38380089
hg19380089
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426195
Supporting Variants
Samples
Known GenesC9orf66, CBWD1, DOCK8, FOXD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231684
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00011


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