A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18265446



Internal ID20832486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:95357291..95357772hg38UCSC Ensembl
chr4:96278442..96278923hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38482
hg19482
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567545
Supporting Variants
Samples
Known GenesUNC5C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18265446
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00011


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