A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18263441



Internal ID20830481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1056480..1181419hg38UCSC Ensembl
chr4:1050268..1175207hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg38124940
hg19124940
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6571930
Supporting Variants
Samples
Known GenesRNF212, SPON2, TMED11P
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18263441
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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