A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18226020



Internal ID20793060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:88092434..88144474hg38UCSC Ensembl
chr9:90707349..90759389hg19UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg3852041
hg1952041
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440027
Supporting Variants
Samples
Known GenesSPATA31C2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18226020
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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