A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18178382



Internal ID20745422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:69077704..69079973hg38UCSC Ensembl
chr9:71692620..71694889hg19UCSC Ensembl
Cytoband9q21.11
Allele length
AssemblyAllele length
hg382270
hg192270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6437306
Supporting Variants
Samples
Known GenesFXN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18178382
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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