A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18268361



Internal ID20835401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:42104687..42104809hg38UCSC Ensembl
chr5:42104789..42104911hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6562318
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18268361
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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