A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218821



Internal ID20785861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128622863..128637553hg38UCSC Ensembl
chr9:131385142..131399832hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3814691
hg1914691
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441315
Supporting Variants
Samples
Known GenesSPTAN1, WDR34
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218821
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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