A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18234998



Internal ID20802038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:63695801..63862700hg38UCSC Ensembl
chr9:68291535..68458434hg19UCSC Ensembl
Cytoband9q13
Allele length
AssemblyAllele length
hg38166900
hg19166900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446660
Supporting Variants
Samples
Known GenesLOC642236
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18234998
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.49752


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