A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235618



Internal ID20802658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:102591799..102708895hg38UCSC Ensembl
chr9:105354081..105471177hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38117097
hg19117097
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6438228
Supporting Variants
Samples
Known GenesLINC00587
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235618
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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