A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18264872



Internal ID20831912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:157275158..157418735hg38UCSC Ensembl
chr4:158196310..158339887hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38143578
hg19143578
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6573298
Supporting Variants
Samples
Known GenesGRIA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18264872
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.00039


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