A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18232760



Internal ID20799800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128817601..128819800hg38UCSC Ensembl
chr9:131579880..131582079hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448188
Supporting Variants
Samples
Known GenesC9orf114, ENDOG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18232760
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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