A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229153



Internal ID20796193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:118806501..118811600hg38UCSC Ensembl
chr9:121568779..121573878hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6450895
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229153
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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