A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18262996



Internal ID20830036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:109567446..109567654hg38UCSC Ensembl
chr4:110488602..110488810hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38209
hg19209
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6560367
Supporting Variants
Samples
Known GenesCCDC109B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18262996
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.0005


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