A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177552



Internal ID20744592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:93346007..93348304hg38UCSC Ensembl
chr9:96108289..96110586hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg382298
hg192298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442511
Supporting Variants
Samples
Known GenesC9orf129
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177552
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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