A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231811



Internal ID20798851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63783901..63862600hg38UCSC Ensembl
chr9:68379635..68458334hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg3878700
hg1978700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6454572
Supporting Variants
Samples
Known GenesLOC642236
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231811
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.80633


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