A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18176287



Internal ID20743327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:121195980..121196291hg38UCSC Ensembl
chr9:123958258..123958569hg19UCSC Ensembl
Cytoband9q33.2
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6442788
Supporting Variants
Samples
Known GenesRAB14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18176287
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00201


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