A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264025



Internal ID20831065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:69100589..69101322hg38UCSC Ensembl
chr3:69149740..69150473hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg38734
hg19734
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540457
Supporting Variants
Samples
Known GenesARL6IP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264025
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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