A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18250360



Internal ID20817400
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:231346387..231346947hg38UCSC Ensembl
chr1:231482133..231482693hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg38561
hg19561
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540161
Supporting Variants
Samples
Known GenesSPRTN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18250360
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0


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